Phenylpyridine derivative and drug containing same

ABSTRACT

The present invention provides: a compound represented by general formula (I) below, that has both angiotensin II receptor antagonism and a PPARγ activation effect and that is useful as a preventative and/or therapeutic agent for high blood pressure, cardiac disease, arteriosclerosis, type-2 diabetes, and the like; and a drug composition containing the compound. General formula (I) (in the formula: ring A represents a pyridine ring; ring B represents a tetrazole ring or an oxadiazol-5(4H)-one ring; X represents C—R 5  or a nitrogen atom; R 1  represents an alkyl group; R 2  represents an alkyl group or a cycloalkyl group; and R 3 , R 4 , and R 5  each independently represents a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group or similar.

TECHNICAL FIELD

The present invention relates to novel phenylpyridine derivatives thathave both angiotensin II antagonistic activity and a PPARγ activationeffect, and a pharmaceutical agent containing the same.

BACKGROUND ART

In recent years, diseases such as diabetes, hypertension, dyslipidemiaand obesity which can be a risk factor for arteriosclerotic diseaseshave been rapidly increasing due to changes in life style withimprovements in living standard, i.e., high calorie and high cholesteroltype diet, obesity, lack of exercise, aging, and the like. It is knownthat, although being a risk factor independent of each other, overlap ofthe diseases can cause an occurrence of arteriosclerotic diseases athigher frequency or aggravation of the diseases. As such, with theunderstanding of a condition having a plurality of risk factors forarteriosclerotic diseases as metabolic syndrome, efforts have been madeto elucidate the cause of the syndrome and to develop a therapeuticmethod therefor.

Angiotensin II (herein below, also abbreviated as “AII”) is a peptidethat is found to be an intrinsic pressor substance produced byrenin-angiotensin system (i.e., RA system). It is believed thatpharmacological inhibition of angiotensin II activity can lead totreatment or prevention of circulatory diseases such as hypertension.Accordingly, an inhibitor for angiotensin converting enzyme (ACE) whichinhibits the enzyme for promoting the conversion of angiotensin I (AI)to angiotensin II has been clinically used as an inhibitory agent for RAsystem. Furthermore, an orally administrable AII receptor blocker(Angiotensin Receptor Blocker: ARB) has been developed, and losartan,candesartan, telmisartan, valsartan, olmesartan, irbesartan, and thelike are already clinically used as a hypotensive agent. It is reportedby many clinical or basic studies that, as having not only a hypotensiveactivity but also other various activities including ananti-inflammatory activity, an endothelial function improving activity,a cardiovascular remodeling inhibiting activity, an oxidation stressinhibiting activity, a proliferation factor inhibiting activity, insulinresistance improving activity, and the like, ARB is useful forcardiovascular diseases, renal diseases, arteriosclerosis, and the like(Non-Patent Documents 1 and 2). Most recently, it is also reported thatARB particularly has a kidney protecting activity which does not dependon a hypotensive activity (Non-Patent Document 3).

Meanwhile, three isoforms, i.e., α, γ and δ have been identified so farfor peroxisome proliferator-activated receptors (PPARs) which belong toa nuclear receptor superfamily. Among them, PPARγ is an isoform mostabundantly expressed in an adipose tissue and it plays an important rolein differentiation of adipocytes or metabolism of glycolipids.Currently, thiazolidinedione derivatives (i.e., TZD) such aspioglitazone or rosiglitazone are clinically used as a therapeutic agentfor diabetes having a PPARγ activation effect, and they are known tohave an activity of improving insulin resistance, glucose tolerance,lipid metabolism, and the like. Further, it is recently reported that,based on activation of PPARγ, TZD exhibits various activities includinga hypotensive activity, an anti-inflammatory activity, an endothelialfunction improving activity, a proliferation factor inhibiting activity,an activity of interfering RA system, and the like. It is also reportedthat, according to such multiple activities, TZD shows a kidneyprotecting activity particularly in diabetic nephropathy withoutdepending on blood sugar control (Non-Patent Documents 4, 5, 6, 7, and8). Meanwhile, there is also a concern regarding adverse effects of TZDcaused by PPARγ activation, such as body fluid accumulation, body weightgain, peripheral edema, and pulmonary edema (Non-Patent Documents 9 and10).

It has been recently reported that telmisartan has a PPARγ activationeffect (Non-Patent Document 11). It has been also reported that theirbesartan has the same activity (Non-Patent Document 12). Thesecompounds have both an RA system inhibiting activity and a PPARγactivation effect, and thus are expected to be used as an integratedagent for prevention and/or treatment of circulatory diseases (e.g.,hypertension, heart disease, angina pectoris, cerebral vasculardisorder, cerebral circulatory disorder, ischemic peripheral circulatorydisorder, kidney disease, and the like) or diabetes-related diseases(e.g., type 2 diabetes mellitus, diabetic complication, insulinresistant syndrome, metabolic syndrome, hyperinsulinemia, and the like)without increasing a risk of body fluid accumulation, body weight gain,peripheral edema, pulmonary edema, or congestive heart failure that areconcerned over the use of TZD (Patent Document 1). Among them, fordiabetic nephropathy, a synergistic prophylactic and/or therapeuticeffect is expected from composite kidney protecting activity that isbased on activities of RA system inhibition and PPARγ activation.

As a compound having the activities above, pyrimidine and triazinederivatives (Patent Document 1), imidazopyridine derivatives (PatentDocument 2), indole derivatives (Patent Document 3), imidazolederivatives (Patent Document 4), and condensed ring derivatives (PatentDocument 5) have been reported. However, there is no description orsuggestion regarding the phenylpyridine derivatives of the presentinvention.

Meanwhile, Patent Document 6 discloses a compound represented by thefollowing formula (A):

[in the formula, R¹ is an optionally substituted hydrocarbon residuewhich is optionally bonded through a hetero atom, R² is an optionallysubstituted 5 to 7 membered heterocyclic residue having, as a groupcapable of constituting the ring, a carbonyl group, a thiocarbonylgroup, an optionally oxidized sulfur atom or a group convertible intothem, X is a direct bond or bonding via a spacer having an atomic lengthof two or less between the ring Y and the ring W, W and Y are anoptionally substituted aromatic hydrocarbon residue optionallycontaining a hetero atom or an optionally substituted heterocyclicresidue; n is an integer of 1 or 2, a and b forming the heterocyclicresidue are independently one or two optionally substituted carbon orhetero atoms, c is an optionally substituted carbon or hetero atom, and,in the group of the formula,

substituent groups on adjacent two atoms forming the ring are optionallybonded to each other to form a 5 to 6 membered ring together with thetwo atoms forming the ring]. As a preferred W—Y ring system, biphenyl isexemplified. In the Examples, only the biphenyl derivatives arespecifically described. The compounds disclosed in Patent Document 6 aredifferent from the compounds of the present invention in terms of thering bonded to the pyridinyl methyl group. In addition, Patent Document6 includes no descriptions or suggestions relating to a PPARγ activationeffect as a pharmacological activity or treatment of diabetes, obesity,or metabolic syndromes.

PRIOR ART DOCUMENT Patent Document

-   Patent Document 1: WO 2008/062905 A-   Patent Document 2: WO 2008/084303 A-   Patent Document 3: WO 2008/096820 A-   Patent Document 4: WO 2008/096829 A-   Patent Document 5: WO 2008/143262 A-   Patent Document 6: JP 5-271228 A

Non-Patent Document

-   Non-Patent Document 1: AMER. J. Hypertension, 18, 720 (2005)-   Non-Patent Document 2: Current Hypertension Report, 10, 261 (2008)-   Non-Patent Document 3: Diabetes Care, 30, 1581 (2007)-   Non-Patent Document 4: Kidney Int., 70, 1223 (2006)-   Non-Patent Document 5: Circulation, 108, 2941 (2003)-   Non-Patent Document 6: Best Pract. Res. Clin. Endocrinol. Metab., 21    (4), 687 (2007)-   Non-Patent Document 7: Diab. Vasc. Dis. Res., 1 (2), 76 (2004)-   Non-Patent Document 8: Diab. Vasc. Dis. Res., 2 (2), 61 (2005)-   Non-Patent Document 9: J. Clin. Invest., 116 (3), 581 (2006)-   Non-Patent Document 10: FASEB J., 20 (8), 1203 (2006)-   Non-Patent Document 11: Hypertension, 43, 993 (2004)-   Non-Patent Document 12: Circulation, 109, 2054 (2004)

SUMMARY OF THE INVENTION Problems to be Solved by the Invention

An object of the invention is to provide a novel compound that is usefulas a pharmaceutical agent for preventing and/or treating hypertension asa circulatory disease, diabetes as a metabolic disease, and the like,and a pharmaceutical composition using the novel compound.

Means for Solving the Problems

As a result of intensive studies to achieve the purpose described above,the inventors found that the compound represented by the formula (I)below has both an excellent angiotensin II antagonistic activity and anexcellent PPARγ activation effect, and therefore completed theinvention.

Specifically, the present invention relates to the following inventions.

[1] A compound represented by the formula (I) below or a salt thereof,or a solvate thereof:

[in the formula, ring A represents the following formula (II) or formula(III):

ring B represents the following formula (IV) or formula (V):

X represents C—R⁵ or a nitrogen atom,

R¹ represents a C₁₋₆ alkyl group,

R² represents a C₁₋₆ alkyl group or a C₃₋₈ cycloalkyl group, and

R³, R⁴, and R⁵ each independently represent a hydrogen atom, a halogenatom, a C₁₋₆ alkyl group, a halo C₁₋₆ alkyl group, or a C₁₋₆ alkoxygroup which may have a substituent group, and the broken line in theformula indicates the binding site for a neighboring group].

[2] The compound described in the above [1] or a salt thereof, or asolvate thereof, in which the ring A in the formula (I) is the formula(II) described above, and X is a nitrogen atom.

[3] The compound described in the above [1] or [2] or a salt thereof, ora solvate thereof, in which the ring B in the formula (I) is the formula(V) described above.

[4] The compound described in any one of the above [1] to [3] or a saltthereof, or a solvate thereof, in which R² in the formula (I) is abranched C₁₋₆ alkyl group or a C₃— cycloalkyl group.

[5] The compound described in any one of the above [1] to [4] or a saltthereof, or a solvate thereof, in which R¹ in the formula (I) is a C₁₋₃alkyl group or a C₅₋₆ alkyl group.

[6] The compound described in any one of the above [1] to [5] or a saltthereof, or a solvate thereof, in which the ring A in the formula (I) isthe formula (II) described above and the ring B is the formula (V)described above.

[7] The compound described in any one of the above [1] to [6] or a saltthereof, or a solvate thereof, in which X in the formula (I) is anitrogen atom and R³ and R⁴ are each independently a hydrogen atom, ahalogen atom, a C₁₋₆ alkyl group, a halo C₁₋₆ alkyl group, or a C₁₋₆alkoxy group.

[8] The compound described in the above [7] or a salt thereof, or asolvate thereof, in which R³ and R⁴ in the formula (I) are eachindependently a hydrogen atom or a C₁₋₆ alkoxy group.

[9] The compound described in the above [1] or a salt thereof, or asolvate thereof, in which the compound represented by the formula (I) isa compound selected from a group consisting of:

-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-methoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-ethyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-ethylpyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-isopropyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-isopropylpyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclopropyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclobutyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclobutyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclopentyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclohexyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-methyl-3-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-methyl-3-{5-[2-(methylsulfonyl)ethoxy]pyrimidin-2-yl}pyrimidin-4(3H)-one,-   3-{2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-methyl-1-(4-methylpyridin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-ethyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-isopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclobutyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclobutyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclopentyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclohexyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylsulfonyl)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-2-methyl-3-(pyridin-2-yl)pyrimidin-4(3H)-one,-   5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(5-methoxypyridin-2-yl)-2-methylpyrimidin-4(3H)-one,-   5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]-2-methylpyrimidin-4(3H)-one,-   5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(5-methoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one,-   5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one,-   5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(4,6-dimethoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one,-   3-{2-{6-{[4-butyl-1-(5-methoxypyridin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{6-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{6-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{6-{[4-butyl-1-(4,6-dimethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-4-ethyl-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,    and-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-4-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one.

[10] The compound described in the above [1] or a salt thereof, or asolvate thereof, in which the compound represented by the formula (I) isa compound selected from a group consisting of:

-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-isopropyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-isopropylpyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclopropyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclobutyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclobutyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclopentyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclohexyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   3-{2-{5-{[4-butyl-2-isopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclobutyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclobutyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclopentyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclohexyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-4-ethyl-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,    and-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-4-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one.

[11] The compound described in the above [1] or a salt thereof, or asolvate thereof, in which the compound represented by the formula (I) isa compound selected from a group consisting of:

-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-4-ethyl-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,    and-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-4-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one.

Meanwhile, the alkyl group such as butyl in the nomenclature of theabove-mentioned compounds represents a straight (normal) chain unlessparticularly described.

[12] A pharmaceutical composition containing the compound described inany one of the above [1] to [11] or a salt thereof, or a solvatethereof, and a pharmaceutically acceptable carrier.

[13] The pharmaceutical composition described in the above [12], inwhich the ring A in the formula (I) is the formula (II) described aboveand X is a nitrogen atom.

[14] The pharmaceutical composition described in the above [12] or[1,3], in which the ring B in the formula (I) is the formula (V)described above.

[15] The pharmaceutical composition described in any one of the above[12] to [14], in which R² in the formula (I) is a branched C₃₋₆ alkylgroup or a C₃₋₈ cycloalkyl group.

[16] The pharmaceutical composition described in any one of the above[12] to [15], in which R¹ in the formula (I) is a C₁₋₃ alkyl group or aC₅₋₆ alkyl group.

[17] The pharmaceutical composition described in any one of the above[12] to [16], in which the ring A in the formula (I) is the formula (II)described above and the ring B is the formula (V) described above.

[18] The pharmaceutical composition described in any one of the above[12] to [17], in which X in the formula (I) is a nitrogen atom and R³and R⁴ are each independently a hydrogen atom, a halogen atom, a C₁₋₆alkyl group, a halo C₁₋₆ alkyl group, or a C₁₋₆ alkoxy group.

[19] The pharmaceutical composition described in the above [18], inwhich R³ and R⁴ in the formula (I) are each independently a hydrogenatom or a C₁₋₆ alkoxy group.

[20] The pharmaceutical composition described in any one of the above[12] to [19], having both angiotensin II receptor antagonistic activityand a PPARγ activation effect.

[21] The pharmaceutical composition described in any one of the above[12] to [20], which is an agent for preventing and/or treating acirculatory disease.

[22] The pharmaceutical composition described in the above [21], inwhich the circulatory disease is hypertension, heart disease, anginapectoris, cerebral vascular disorder, cerebral circulatory disorder,ischemic peripheral circulatory disorder, kidney disease, orarteriosclerosis.

[23] The pharmaceutical composition described in any one of the above[12] to [20], which is an agent for preventing and/or treating ametabolic disease.

[24] The pharmaceutical composition described in the above [23], inwhich the metabolic disease is type 2 diabetes mellitus, diabeticcomplication (diabetic retinopathy, diabetic neuropathy, or diabeticnephropathy), insulin resistant syndrome, metabolic syndrome, orhyperinsulinemia.

[25] A method of preventing and/or treating a circulatory disease, themethod including administering an effective amount of the compounddescribed in any one of the above [1] to [11] or a salt thereof, or asolvate thereof to a patient who is in need of the treatment.

[26] The method described in the above [25], in which the circulatorydisease is hypertension, heart disease, angina pectoris, cerebralvascular disorder, cerebral circulatory disorder, ischemic peripheralcirculatory disorder, kidney disease, or arteriosclerosis.

[27] A method of preventing and/or treating a metabolic disease, themethod including administering an effective amount of the compounddescribed in any one of the above [1] to [11] or a salt thereof, or asolvate thereof to a patient who is in need of the treatment.

[28] The method described in the above [27], in which the metabolicdisease is type 2 diabetes mellitus, diabetic complication (diabeticretinopathy, diabetic neuropathy, or diabetic nephropathy), insulinresistant syndrome, metabolic syndrome, or hyperinsulinemia.

[29] A method of preventing and/or treating a circulatory disease and ametabolic disease, the method including administering an effectiveamount of the compound described in any one of the above [1] to [11] ora salt thereof, or a solvate thereof to a patient who is in need of thetreatment.

[30] The method described in the above [29], in which the circulatorydisease is hypertension, heart disease, angina pectoris, cerebralvascular disorder, cerebral circulatory disorder, ischemic peripheralcirculatory disorder, kidney disease, or arteriosclerosis and themetabolic disease is type 2 diabetes mellitus, diabetic complication(diabetic retinopathy, diabetic neuropathy, or diabetic nephropathy),insulin resistant syndrome, metabolic syndrome, or hyperinsulinemia.

[31] Use of the compound described in any one of the above [1] to [11]or a salt thereof, or a solvate thereof for producing a preparation forpreventing and/or treating a circulatory disease.

[32] The use described in the above [31], in which the circulatorydisease is hypertension, heart disease, angina pectoris, cerebralvascular disorder, cerebral circulatory disorder, ischemic peripheralcirculatory disorder, kidney disease, or arteriosclerosis.

[33] Use of the compound described in any one of the above [1] to [11]or a salt thereof, or a solvate thereof for producing a preparation forpreventing and/or treating a metabolic disease.

[34] The use described in the above [33], in which the metabolic diseaseis type 2 diabetes mellitus, diabetic complication (diabeticretinopathy, diabetic neuropathy, or diabetic nephropathy), insulinresistant syndrome, metabolic syndrome, or hyperinsulinemia.

[35] The compound described in any one the above [1] to [11] or a saltthereof, or a solvate thereof to be used for a pharmaceuticalcomposition for preventing and/or treating a circulatory disease.

[36] The compound described in the above [35] or a salt thereof, or asolvate thereof, in which the circulatory disease is hypertension, heartdisease, angina pectoris, cerebral vascular disorder, cerebralcirculatory disorder, ischemic peripheral circulatory disorder, kidneydisease, or arteriosclerosis.

[37] The compound described in the above [35] or [36] or a salt thereof,or a solvate thereof, in which the effective component of apharmaceutical composition is a compound or a salt thereof, or a solvatethereof having both an angiotensin II receptor antagonistic activity anda PPARγ activation effect.

[38] The compound described in any one of the above [1] to [11] or asalt thereof, or a solvate thereof to be used for a pharmaceuticalcomposition for preventing and/or treating a metabolic disease.

[39] The compound described in the above [38] or a salt thereof, or asolvate thereof, in which the metabolic disease is type 2 diabetesmellitus, diabetic complication (diabetic retinopathy, diabeticneuropathy, or diabetic nephropathy), insulin resistant syndrome,metabolic syndrome, or hyperinsulinemia.

[40] The compound described in the above [38] or [39] or a salt thereof,or a solvate thereof, in which the effective component of apharmaceutical composition is a compound or a salt thereof, or a solvatethereof having both an angiotensin II receptor antagonistic activity anda PPARγ activation effect.

[41] The compound described in any one of the above [1] to [11] or asalt thereof, or a solvate thereof to be used for a pharmaceuticalcomposition for preventing and/or treating a circulatory disease or ametabolic disease.

[42] The compound described in the above [41] or a salt thereof, or asolvate thereof, in which the circulatory disease is hypertension, heartdisease, angina pectoris, cerebral vascular disorder, cerebralcirculatory disorder, ischemic peripheral circulatory disorder, kidneydisease, or arteriosclerosis and the metabolic disease is type 2diabetes mellitus, diabetic complication (diabetic retinopathy, diabeticneuropathy, or diabetic nephropathy), insulin resistant syndrome,metabolic syndrome, or hyperinsulinemia.

Effects of the Invention

The phenylpyridine derivative represented by the formula (I) of theinvention or a salt thereof, or a solvate thereof exhibits a potentantagonistic activity for an angiotensin II receptor, and can beappropriately used as an effective component of an agent for preventingand/or treating a disease related with angiotensin II, for example acirculatory disease such as hypertension, heart disease, anginapectoris, cerebral vascular disorder, cerebral circulatory disorder,ischemic peripheral circulatory disorder, kidney disease, andarteriosclerosis.

Further, the phenylpyridine derivative represented by the formula (I) ofthe invention or a salt thereof, or a solvate thereof exhibits a PPARγactivation effect and can be appropriately used as an effectivecomponent of an agent for preventing and/or treating a disease relatedwith PPARγ, for example a metabolic disease such as arteriosclerosis,type 2 diabetes mellitus, diabetic complication (diabetic retinopathy,diabetic neuropathy, or diabetic nephropathy), insulin resistancesyndrome, syndrome X, metabolic syndrome, and hyperinsulinemia.

Still further, the phenylpyridine derivative represented by the formula(I) of the invention or a salt thereof, or a solvate thereof has both anantagonistic activity for an angiotensin II receptor and a PPARγactivation effect and can be appropriately used as an effectivecomponent of an agent for preventing and/or treating a disease relatedwith both angiotensin II and PPARγ, for example, arteriosclerosis,diabetic nephropathy, insulin resistance syndrome, syndrome X, andmetabolic syndrome.

MODES FOR CARRYING OUT THE INVENTION

The “halogen atom” as used herein includes a fluorine atom, a chlorineatom, a bromine atom, an iodine atom, and the like.

The “C₁₋₆ alkyl group” and “C₁₋₆ alkyl” as used herein mean a linear ora branched hydrocarbon group having 1 to 6 carbon atoms, preferably asaturated linear or branched hydrocarbon group having 1 to 6 carbonatoms, and examples thereof include a methyl group, an ethyl group, ann-propyl group, an isopropyl group, an n-butyl group, an isobutyl group,a t-butyl group, an n-pentyl group, a 2-methylbutyl group, a2,2-dimethylpropyl group, and an n-hexyl group. Further, the “branchedC₃₋₆ alkyl group” and “branched C₃₋₆ alkyl” as used herein mean abranched hydrocarbon group having 3 to 6 carbon atoms, preferably asaturated branched hydrocarbon group having 3 to 6 carbon atoms, andexamples thereof include an isopropyl group, an isobutyl group, a2-methylbutyl group, a 2-methylpentyl group, and a 2-ethylbutyl group.

The “C₃₋₈ cycloalkyl group” and “C₃₋₈ cycloalkyl” as used herein mean asaturated or unsaturated and monocyclic, polycyclic, or fused-cycliccycloalkyl group having 3 to 8 carbon atoms, and preferably 3 to 6carbon atoms, and examples of the cycloalkyl group include a cyclopropylgroup, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, acycloheptyl group, and a cyclooctyl group.

The “halo C₁₋₆ alkyl group” and “halo C₁₋₆ alkyl” as used herein mean alinear or a branched alkyl group having 1 to 6 carbon atoms which issubstituted with one or more to maximally substitutable number ofhalogen atoms, and examples thereof include a fluoromethyl group, adifluoromethyl group, a trifluoromethyl group, a 2,2,2-trifluoroethylgroup, a 1,1,2,2,2-pentafluoroethyl group, and a 3,3,3-trifluoropropylgroup.

The “C₁₋₆ alkoxy group” as used herein means a linear or a branchedalkoxy group having 1 to 6 carbon atoms, and examples thereof include amethoxy group, an ethoxy group, a propoxy group, an isopropoxy group, abutoxy group, an isobutoxy group, a sec-butoxy group, a tert-butoxygroup, a pentoxy group, an isopentoxy group, a neopentoxy group, ahexyloxy group, and an isohexyloxy group.

As used herein, the “substituent group” of the “C₁₋₅ alkoxy group whichmay have a substituent group” may be the same or different from eachother, and the alkoxy group may be substituted with one or more tomaximally substitutable number of substituent groups. Examples of the“substituent group” include a phenyl group, a hydroxyl group, a C₁₋₆alkoxy group, a C₁₋₆ alkylthio group, a C₁₋₆ alkylsulfonyl group, anoxazolyl group (the oxazolyl group may be substituted with a C₁₋₆ alkylgroup, a C₆₋₁₀ aryl group, or a 5 to 10-membered heteroaryl group whichmay be substituted with a halogen atom), a pyridyl group (the pyridylgroup may be substituted with a C₁₋₆ alkyl group), a C₁₋₆ alkoxycarbonylgroup, a carboxyl group, a carbamoyl group, a mono C₁₋₆ alkylcarbamoylgroup, a di C₁₋₆ alkylcarbamoyl group, a C₁₋₆ alkanoylamino group, aC₁₋₆ alkylsulfonylamino group, a halo C₁₋₆ alkylsulfonylamino group, anamide group, and a sulfonamide group. Preferred examples of thesubstituent group include a C₁₋₆ alkylthio group, a C₁₋₆ alkylsulfonylgroup, a carboxyl group, a carbamoyl group, a mono C₁₋₆ alkylcarbamoylgroup, and a di C₁₋₆ alkylcarbamoyl group. Still more preferred examplesof the substituent group include a C₁₋₆ alkylthio group and a C₁₋₆alkylsulfonyl group.

Preferred modes of the invention include those described below.

In the formula (I), the C₁₋₆ alkyl group as R¹ is preferably a C₁₋₆alkyl group except butyl group, that is, a C₁₋₃ alkyl group or a C₅₋₆alkyl group, and examples thereof include an ethyl group, an n-propylgroup, and an n-pentyl group.

In the formula (I), the C₁₋₆ alkyl group as R² is preferably a C₁₋₄alkyl group, and examples thereof include a methyl group, an ethylgroup, and an isopropyl group. An isopropyl group is particularlypreferable. Preferred examples of the C₁₋₆ alkyl group as R² include abranched C₃₋₆ alkyl group. An isopropyl group is particularlypreferable.

In the formula (I), preferred examples of the C₃₋₈ cycloalkyl group asR² include C₃₋₆ cycloalkyl, for example, a cyclopropyl group, acyclobutyl group, a cyclopentyl group, and a cyclohexyl group. Acyclopropyl group is particularly preferable.

In the formula (I), preferred examples of the C₁₋₆ alkyl group as R³ andR⁴ include a C₁₋₄ alkyl group, for example, a methyl group and an ethylgroup.

In the formula (I), preferred examples of the halo C₁₋₆ alkyl group asR¹ and R⁴ include a halo C₁₋₄ alkyl group, for example, a difluoromethylgroup, a trifluoromethyl group, and a 2,2,2-trifluoroethyl group. Atrifluoromethyl group is more preferable.

In the formula (I), preferred examples of the “C₁₋₆ alkoxy group” of theC₁₋₆ alkoxy group which may have a substituent group as R³ and R⁴include a C₁₋₄ alkoxy group, for example, a methoxy group, an ethoxygroup, a propoxy group, an isopropoxy group, and an n-butoxy group. Anethoxy group is particularly preferable. Preferred examples of the“substituent group” include a phenyl group, a hydroxyl group, a C₁₋₆alkylthio group (for example, a methylthio group), and a C₁₋₆alkylsulfonyl group (for example, a methylsulfonyl group).

More preferred examples of the compound represented by the formula (I)include a compound selected from a group consisting of the followingcompounds:

-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-methoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-ethyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-ethylpyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-isopropyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-isopropylpyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclopropyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclobutyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclobutyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclopentyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclohexyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-methyl-3-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-methyl-3-{5-[2-(methylsulfonyl)ethoxy]pyrimidin-2-yl}pyrimidin-4(3H)-one,-   3-{2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-methyl-1-(4-methylpyridin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-ethyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-isopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclobutyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclobutyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclopentyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclohexyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylsulfonyl)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-2-methyl-3-(pyridin-2-yl)pyrimidin-4(3H)-one,-   5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(5-methoxypyridin-2-yl)-2-methylpyrimidin-4(3H)-one,-   5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]-2-methylpyrimidin-4(3H)-one,-   5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(5-methoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one,-   5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one,-   5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(4,6-dimethoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one,-   3-{2-{6-{[4-butyl-1-(5-methoxypyridin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{6-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{6-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{6-{[4-butyl-1-(4,6-dimethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-4-ethyl-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,    and-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-4-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one.

More preferred examples of the 5-(pyridinylmethyl)pyrimidin-4(3H)-onederivatives that are represented by the formula (I) include a compoundselected from a group consisting of the following compounds:

-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-isopropyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-isopropylpyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclopropyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclobutyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclobutyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclopentyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclohexyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one,-   3-{2-{5-{[4-butyl-2-isopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclobutyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclobutyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclopentyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[4-butyl-2-cyclohexyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-4-ethyl-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,    and-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-4-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one.

Still more preferred examples of the5-(pyridinylmethyl)pyrimidin-4(3H)-one derivatives that are representedby the formula (I) include a compound selected from a group consistingof the following compounds:

-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,-   3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-4-ethyl-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,    and-   3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-4-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one.

If the compound of the invention has geometrical isomers or opticalisomers, all of such isomers are within the scope of the invention.Isolation of these isomers is carried out by an ordinary method.

Salts of the compound represented by the formula (I) are notparticularly limited, if they are pharmaceutically acceptable salts.When the compound is processed as an acidic compound, an alkali metalsalt or an alkali earth metal salt such as sodium salt, potassium salt,magnesium salt, and calcium salt, and the like; and a salt with anorganic base such as trimethylamine, triethylamine, pyridine, picoline,N-methyl pyrrolidine, N-methyl piperidine, N-methyl morpholine, and thelike can be mentioned. When the compound is processed as a basiccompound, an acid addition salt and the like including a salt with amineral acid, for example, hydrochloric acid salt, hydrobromic acidsalt, hydroiodic acid salt, sulfuric acid salt, nitric acid salt,phosphoric acid salt, and the like; or organic acid addition salt, forexample, benzoic acid salt, methanesulfonic acid salt, ethanesulfonicacid salt, benzenesulfonic acid salt, p-toluene sulfonic acid salt,maleic acid salt, fumaric acid salt, tartaric acid salt, citric acidsalt, and acetic acid salt; or the like can be mentioned.

Examples of the solvate of the compound represented by the formula (I)or a salt thereof include a hydrate, but not limited thereto.

In addition, compounds which are metabolized in a living body andconverted into the compounds represented by the aforementioned formula(I), so called prodrugs, all fall within the scope of the compounds ofthe invention. Examples of groups which form the prodrugs of thecompounds of the invention include the groups described in “Progress inMedicine”, Vol. 5, pp. 2157-2161, 1985, Life Science Medica, and thegroups described in “Development of Drugs”, Vol. 7, Molecular Designs,pp. 163-198, published in 1990, Hirokawa Shoten.

The compounds represented by the formula (I) or salts thereof, orsolvates thereof can be produced according to various known methods, andthe production method is not specifically limited. For example, thecompounds can be produced according to the following reaction process.Further, when each reaction described below is performed, functionalgroups other than the reaction sites may be protected beforehand asrequired, and deprotected in an appropriate stage. Furthermore, thereaction in each process may be performed by an ordinarily used method,and isolation and purification can be performed by a method suitablyselected from conventional methods such as crystallization,recrystallization, chromatography, or the like, or a combinationthereof.

(Production Method)

1. Method for Production of the Compound (Ia) in which the Ring B is theFormula (IV)

Among the compounds represented by the formula (I) of the invention, thecompound represented by the formula (Ia) can be produced according tothe following method, but it is not limited thereto. Specifically, asdescribed in the following Reaction pathway 1, if pyridinyl methylhalide (VI) and β-ketoester (VII) are reacted with each other and theobtained compound (VIII) are reacted with ammonium acetate followed byreaction with acid anhydride (IX) or acid chloride (X), acylaminocompound (XI) is obtained. If the acylamino compound (XI) is reactedwith amino compound (XII), pyrimidinone derivative (XIII) is obtained.If the pyrimidinone derivative (XIII) is reacted with an azide compound,the compound represented by the formula (Ia) of the invention can beobtained.

[Reaction Pathway 1]

(in the formula, ring A, R¹, R², R³, R⁴, and X are as defined above, R⁶represents a protecting group for carboxyl group such as C₁₋₈ alkylgroup, and W represents a leaving group such as halogen atom).

[Process 1] The reaction between the pyridinyl methyl halide (VI) andthe β-ketoester (VII) may be carried out in a solvent in the presence ofa base and lithium halide (lithium chloride, lithium bromide, and thelike). The solvent is not specifically limited, and N,N-dimethylformamide, N-methyl pyrrolidone, dimethyl sulfoxide, dioxane,tetrahydrofuran, acetonitrile, and propionitrile may be used eitheralone or in combination thereof. The base is not specifically limited,and examples thereof which may be used include an organic base such aspyridine, N,N-dimethylaminopyridine (DMAP), collidine, lutidine,1,8-diazabicyclo[5.4.0]-7-undecene (DBU),1,5-diazabicyclo[4.3.0]-5-nonene (DBN), 1,4-diazabicyclo[2.2.2]octane(DABCO), triethylamine, diisopropylamine, diisopropylethylamine,diisopropylpentylamine, and trimethylamine, an alkali metal hydride suchas lithium hydride, sodium hydride, and potassium hydride, an alkalimetal hydroxide such as lithium hydroxide, sodium hydroxide, andpotassium hydroxide, an alkali metal carbonate such as lithiumcarbonate, sodium carbonate, potassium carbonate, and cesium carbonate,and an alkali metal bicarbonate such as sodium hydrogen carbonate. Thereaction condition may vary depending on the reaction materials used.However, the reaction is generally carried out at −20 to 120° C., andpreferably 20° C. to 100° C., for 1 minute to 2 days, and preferably for5 minutes to 36 hours to obtain the compound (VIII).

[Process 2-1] The reaction between the compound (VIII) and ammoniumacetate may be carried out in a solvent in the presence of an acid. Thesolvent is not specifically limited, and methanol, ethanol, isopropanol,ethyl acetate, isopropyl acetate, toluene, benzene, dioxane,tetrahydrofuran, acetonitrile, propionitrile, N,N-dimethylformamide,N-methylpyrrolidone, and dimethyl sulfoxide may be used either alone orin combination thereof. The acid is not specifically limited, andexamples thereof which may be used include a protic acid such as aceticacid, trifluoro acetic acid, propionic acid, and benzoic acid and Lewisacid such as titanium tetrachloride, boron trifluoride, and stannicchloride. The reaction condition may vary depending on the reactionmaterials used. However, the reaction is generally carried out at 0 to180° C., and preferably 50° C. to 150° C., for 1 minute to 24 hours, andpreferably for 5 minutes to 18 hours.

[Process 2-2] The reaction between the crude product obtained afterdistillation of solvent and the acid anhydride (IX) may be carried outin the presence of an acid. The acid is not particularly limited, andexamples thereof which may be used include a protic acid like aceticacid, trifluoroacetic acid, propionic acid, and benzoic acid. Thereaction condition may vary depending on the reaction materials used.However, the reaction is generally carried out at 0 to 180° C., andpreferably 50° C. to 120° C., for 1 minute to 2 days, and preferably for5 minutes to 24 hours to obtain the acylamino compound (XI).

The reaction between the crude product obtained after distillation ofsolvent and the acid chloride (X) may be carried out in a solvent in thepresence or absence of a base. The solvent is not specifically limited,and tetrahydrofuran, toluene, dioxane, N,N-dimethylformamide,N-methylpyrrolidone, 1,2-dichloroethane, dichloromethane, chloroform,acetonitrile, and propionitrile may be used either alone or incombination thereof. The base is not specifically limited, and examplesthereof which may be used include an organic base like pyridine, DMAP,collidine, lutidine, DBU, DBN, DABCO, triethylamine, diisopropylamine,diisopropylethylamine, diisopropylpentylamine, and trimethylamine, analkali metal hydride like lithium hydride, sodium hydride, and potassiumhydride, an alkali metal hydroxide like lithium hydroxide, sodiumhydroxide, and potassium hydroxide, an alkali metal carbonate likelithium carbonate, sodium carbonate, potassium carbonate, and cesiumcarbonate, and sodium hydrogen carbonate. The reaction condition mayvary depending on the reaction materials used. However, the reaction isgenerally carried out at −20 to 100° C., and preferably 15 to 80° C.,for 5 minutes to 48 hours, and preferably for 5 hours to 36 hours toobtain the acylamino compound (XI).

[Process 3] The reaction between the acylamino compound (XI) obtainedaccording to the method above and the amino compound (XII) may becarried out in a solvent in the presence of trialkylaluminum. Thesolvent is not specifically limited, and 1,2-dichloroethane, chloroform,dichloromethane, ethyl acetate, isopropyl acetate, toluene, benzene,tetrahydrofuran, dioxane, acetonitrile, propionitrile, and hexane may beused either alone or in combination thereof. Examples of thetrialkylaluminum which may be used include trimethylaluminum,triethylaluminum, and tripropylaluminum. The reaction condition may varydepending on the reaction materials used. However, the reaction isgenerally carried out at 0 to 150° C., and preferably 50° C. to 120° C.,for 1 minute to 24 hours, and preferably for 5 minutes to 20 hours toobtain the pyrimidinone derivative (XIII).

[Process 4] The reaction between the pyrimidinone derivative (XIII) andan azide compound may be carried out in a solvent. Examples of the azidecompound which may be used include trimethyltin azide, tributyltinazide, triphenyltin azide, sodium azide, and hydrogen azide. Further,trimethylsilyl azide may be used in the presence of dibutyltin oxide.The solvent is not specifically limited, and methanol, ethanol,isopropanol, ethyl acetate, isopropyl acetate, toluene, benzene,dioxane, tetrahydrofuran, acetonitrile, propionitrile,N,N-dimethylformamide, N-methylpyrrolidone, and dimethyl sulfoxide maybe used either alone or in combination thereof. The reaction conditionmay vary depending on the reaction materials used. However, the reactionis generally carried out at 0 to 180° C., and preferably 50 to 120° C.,for 1 minute to 2 weeks, and preferably for 1 hour to 3 days to obtainthe target compound.

2. Method for Production of the Compound (Ib) in which the Ring B is theFormula (V)

Among the compounds represented by the formula (I) of the invention, thecompound represented by the formula (Ib) can be produced according tothe following method, but it is not limited thereto. Specifically, asdescribed in the following Reaction pathway 2, if the pyrimidinonederivative (XIII) and hydroxylamine are reacted with each other, amideoxime product (XIV) is obtained. If the amide oxime product (XIV) isreacted with a carbonyl reagent, the compound represented by the formula(Ib) of the invention can be produced.

[Reaction Pathway 2]

(in the formula, ring A, R¹, R², R³, R⁴, and X are as defined above).

[Process 5] The reaction between the pyrimidinone derivative (XIII) andhydroxylamine may be carried out in a solvent. The solvent is notspecifically limited, and N,N-dimethylformamide, N,N-dimethylacetamide,N-methyl pyrrolidone, dimethyl sulfoxide, methanol, ethanol,isopropanol, 1,4-dioxane, and tetrahydrofuran may be used either aloneor in combination thereof. When an acid salt such as hydroxylaminehydrochloride, hydroxylamine sulfuric acid, hydroxylamine oxalic acid,and the like is used as hydroxylamine, a suitable base, for example,potassium carbonate, sodium hydrogen carbonate, sodium hydroxide,triethylamine, sodium methoxide, sodium hydride, and the like may beused in an equivalent amount or a slightly excess amount for thereaction. The reaction condition may vary depending on the reactionmaterials used. However, the reaction is generally carried out at 0 to180° C., and preferably 50 to 120° C., for 1 minute to 3 days, andpreferably for 1 hour to 36 hours. As a result, the amide oxime product(XIV) is obtained.

[Process 6] Conversion of the amide oxime product (XIV) to the compound(Ib) can be carried out in a solvent in the presence of a base by usinga carbonyl reagent. The solvent is not specifically limited, and1,2-dichloroethane, chloroform, dichloromethane, ethyl acetate,isopropyl acetate, toluene, benzene, tetrahydrofuran, dioxane,acetonitrile, propionitrile, N,N-dimethylformamide,N,N-dimethylacetamide, N-methylpyrrolidone, diethyl ether, or the likemay be used either alone or in combination thereof. The base is notspecifically limited, and examples thereof which may be used includepyridine, DMAP, collidine, lutidine, DBU, DBN, DABCO, triethylamine,diisopropylethylamine, diisopropylpentylamine, trimethylamine, lithiumcarbonate, sodium carbonate, potassium carbonate, cesium carbonate,sodium hydrogen carbonate, potassium hydrogen carbonate, or the like.The carbonyl reagent is not specifically limited, and1,1′-carbonyldiimidazole, triphosgene, methyl chlorocarbonate, ethylchlorocarbonate, or the like may be used. The reaction condition mayvary depending on the reaction materials used. However, the reaction isgenerally carried out at 0 to 120° C., preferably 15 to 80° C. for 5minutes to 3 days, and preferably for 1 hour to 12 hours to obtain thecompound (Ib).

If necessary, the intermediates and target compounds that are obtainedfrom each of the reaction above can be isolated and purified by apurification method that is generally used in a field of organicsynthesis chemistry, for example, filtration, extraction, washing,drying, concentration, recrystallization, various chromatographicmethods, and the like. Furthermore, the intermediates may be used forthe next reaction without any specific purification.

Various isomers may be isolated by applying a general method based on adifference in physicochemical properties among the isomers. For example,a racemic mixture may be resolved into an optically pure isomer bycommon racemic resolution such as optical resolution by which adiastereomer salt is formed with a common optically active acid such astartaric acid or a method of using optically active chromatography.Further, a mixture of diastereomers can be resolved by fractionalcrystallization or various chromatographic methods, for example.Furthermore, an optically active compound can be also produced by usingan appropriate starting compound that is optically active.

The compound (I) obtained may be converted into a salt according to acommon method. Furthermore, the compound (I) or a salt thereof may beconverted into a solvate with a hydrate or a solvate with ethanolaccording to a common method.

Examples of dosage form or administration type of the pharmaceuticalcomposition containing the compounds of the invention or salts thereof,or solvates thereof as an effective component include, for example,those for oral administration such as tablet, capsule, granule, powder,syrup, or the like and those for parenteral administration such asintravenous injection, intramuscular injection, suppository, inhalant,transdermal preparation, eye drop, nasal drop, or the like. In order toprepare a pharmaceutical preparation in the various dosage forms, theeffective component may be used alone, or may be used in appropriatecombination with other pharmaceutically acceptable carriers such asexcipients, binders, extending agents, disintegrating agents,surfactants, lubricants, dispersing agents, buffering agents,preservatives, corrigents, perfumes, coating agents, diluents, and thelike to give a pharmaceutical composition.

Although the administration amount of the pharmaceutical agent of theinvention may vary depending on the weight, age, sex, symptoms, and thelike of a patient, in terms of the compound represented by the formula(I), generally 0.1 to 1000 mg, especially 1 to 300 mg, may beadministered orally or parenterally at one time or several times asdivided portions per day for an adult.

EXAMPLES

Herein below, the invention will be described in greater detail withreference to examples. However, the invention is not limited to theseexamples. The abbreviations used in the examples have the followingmeanings.

s: singlet

d: doublet

t: triplet

q: quartet

m: multiplet

br: broad

J: coupling constant

Hz: Hertz

CDCl₃: deuterated chloroform

DMSO-d₆: deuterated dimethylsulfoxide

¹H-NMR: proton nuclear magnetic resonance

IR: infrared absorption spectrum

Example 1 Preparation of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-methoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one

Process 1: Under argon atmosphere, tetrahydrofuran (900 mL) solution of2-[5-(bromomethyl)pyridin-2-yl]benzonitrile (31.9 g, 117 mmol), methyl3-oxoheptanoate (27.8 g, 176 mmol), diisopropylethylamine (31.0 g, 240mmol), and lithium chloride (8.2 g, 193 mmol) was refluxed under heatingfor 23 hours. The reaction mixture was added water and extracted withethyl acetate. The organic layer was combined, washed with water andbrine, dried over anhydrous sodium sulfate, and concentrated in vacuo.The obtained residues were subjected to silica gel column chromatography(hexane/ethyl acetate=2:1) to give methyl2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxoheptanoate (20.9 g, 51%)as brown oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.87 (3H, t, J=7 Hz), 1.18-1.32 (2H, m), 1.47-1.59 (2H, m), 2.34-2.39(1H, m), 2.55-2.67 (1H, m), 3.20-3.29 (2H, m), 3.73 (3H, s), 3.84 (1H,t, J=7 Hz), 7.50 (1H, td, J=8, 1 Hz), 7.63-7.74 (3H, m), 7.76-7.87 (2H,m), 8.61 (1H, s).

Process 2: Toluene (50 mL)-acetic acid (7 mL) solution of methyl2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxoheptanoate (3.50 g, 10.0mmol) and ammonium acetate (23.2 g, 300 mmol) was refluxed under heatingfor 1 hour. To the residues obtained after distillation of solvent,acetic anhydride (51.2 g) and acetic acid (5.7 g) were added at roomtemperature followed by stirring for 30 minutes at 0° C. and thenstirring for 1.5 hours at 70° C. The reaction mixture was added sodiumbicarbonate water, and then extracted with chloroform. The organic layerwas combined, washed with brine, dried over anhydrous sodium sulfate,and concentrated in vacuo. The obtained residues were subjected tosilica gel column chromatography (hexane/acetone=5:1) to give methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoate(0.975 g, 25%) as pale yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.91 (3H, t, J=7 Hz), 1.33-1.45 (2H, m), 1.46-1.57 (2H, m), 2.18 (3H,s), 2.94 (2H, t, J=6 Hz), 3.71 (3H, s), 3.75 (2H, s), 7.50 (1H, t, J=8Hz), 7.58 (1H, d, J=8 Hz), 7.63-7.72 (2H, m), 7.75-7.83 (2H, m), 8.60(1H, s), 11.9 (1H, s).

Process 3: Under argon atmosphere, trimethylaluminum (2 mol/L hexanesolution, 1.45 mL, 2.90 mmol) was added to 1,2-dichloroethane (30 mL)solution of 2-amino-5-methoxypyrimidine (220 mg, 1.74 mmol) at roomtemperature, and stirred at the same temperature for 80 minutes.1,2-Dichloroethane solution (20 mL) of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoate(227 mg, 0.58 mmol) was added dropwise thereto at room temperature andrefluxed under heating for 17 hours. The reaction mixture was added anaqueous solution of ammonium chloride and chloroform and filteredthrough a pad of celite. The organic layer was separated from thefiltrate and the aqueous layer was extracted with chloroform. Theorganic layer was combined, washed with water and brine, dried overanhydrous sodium sulfate, and concentrated in vacuo. The obtainedresidues were subjected to silica gel column chromatography(hexane/ethyl acetate=2:1) to give2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(207 mg, 77%) as yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.95 (3H, t, J=7 Hz), 1.36-1.48 (2H, m), 1.58-1.70 (2H, m), 2.16 (3H,s), 2.63-2.72 (2H, m), 3.97 (2H, s), 4.01 (2H, s), 7.47 (1H, m),7.60-7.71 (2H, m), 7.72-7.83 (3H, m), 8.54 (2H, s), 8.70 (1H, d, J=1Hz).

Process 4: Trimethylsilyl azide (8.68 g, 75.3 mmol) and dibutyltin oxide(55 mg, 0.221 mmol) were added to toluene (20 mL) solution of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(200 mg, 0.43 mmol) and stirred for 24 hours at 95° C. under argonatmosphere. The residues obtained by removing the reaction solvent bydistillation was separated and purified by silica gel columnchromatography (chloroform:methanol=100:1) to give5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-methoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one(174 mg, 80%) as yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.93 (3H, t, J=7 Hz), 1.33-1.48 (2H, m), 1.55-1.73 (2H, m), 2.16 (3H,s), 2.58-2.72 (2H, m), 3.95 (2H, s), 4.00 (3H, s), 7.20-7.35 (1H, m),7.38-7.58 (3H, m), 7.62-7.82 (1H, m), 8.00-8.22 (1H, m), 8.54 (2H, s),8.50-8.63 (1H, m).

Example 2 Preparation of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one

Process 1: By using 2-amino-5-ethoxypyrimidine instead of2-amino-5-methoxypyrimidine in the Process 3 of the Example 1, thereaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 46%).

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.38-1.46 (2H, m), 1.51 (3H, t, J=7 Hz), 1.60-1.68(2H, m), 2.16 (3H, s), 2.65-2.69 (2H, m), 3.97 (2H, s), 4.22 (2H, q, J=7Hz), 7.47 (1H, m), 7.64-7.81 (5H, m), 8.51 (2H, s), 8.70 (1H, d, J=1Hz).

Process 2: By using2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one(yield: 46%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.38-1.44 (2H, m), 1.51 (3H, t, J=7 Hz), 1.61-1.68(2H, m), 2.17 (3H, s), 2.66-2.70 (2H, m), 3.97 (2H, s), 4.22 (2H, q, J=7Hz), 7.37 (1H, m), 7.48-7.58 (3H, m), 7.78 (1H, m), 8.21 (1H, m), 8.51(2H, s), 8.62 (1H, m).

Example 3 Preparation of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-ethyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one

Process 1: Toluene (36 mL)-acetic acid (4 mL) solution of methyl2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxoheptanoate (1.03 g, 2.94mmol) obtained from the Process 1 of the Example 1 and ammonium acetate(6.80 g, 88.2 mmol) was refluxed under heating for 1 hour. The residuesobtained by removing solvent by distillation were added water and 2mol/L aqueous solution of sodium hydroxide and extracted withchloroform. Propionyl chloride (544 mg, 5.88 mmol) and triethylamine(595 mg, 5.88 mmol) were added to the 1,2-dichloroethane (10 mL)solution of the residues obtained by removing solvent by distillationand stirred for 16 hours at 50° C. The reaction mixture was added waterand extracted with chloroform. The organic layer was combined, washedwith brine, dried over anhydrous sodium sulfate, and concentrated invacuo. The obtained residues were subjected to silica gel columnchromatography (hexane/acetone=5:1) to give methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-propionamide-2-heptenoate(464 mg, 39%) as brown oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.91 (3H, t, J=7 Hz), 1.23 (3H, t, J=8 Hz), 1.34-1.51 (4H, m), 2.43 (2H,q, J=8 Hz), 2.89-2.99 (2H, m), 3.70 (3H, s), 3.75 (2H, s), 7.49 (1H, td,J=8, 1 Hz), 7.58 (1H, dd, J=8, 2 Hz), 7.64-7.73 (2H, m), 7.77-7.86 (2H,m), 8.60 (1H, s), 11.88 (1H, s).

Process 2: By using methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-propionamide-2-heptenoateinstead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoatein the Process 3 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 1 to give2-{5-{[4-butyl-2-ethyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 70%) as a pale yellow solid.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.18 (3H, t, J=7 Hz), 1.35-1.46 (2H, m), 1.62-1.74(2H, m), 2.32 (2H, q, J=7 Hz), 2.69 (2H, t, J=8 Hz), 3.96 (2H, s), 4.00(3H, s), 7.47 (1H, td, J=8, 1 Hz), 7.61-7.70 (2H, m), 7.73-7.82 (3H, m),8.53 (2H, s), 8.69 (1H, s).

Process 3: By using2-{5-{[4-butyl-2-ethyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-ethyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one(yield: 60%) as colorless viscous oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.18 (3H, t, J=7 Hz), 1.34-1.47 (2H, m), 1.60-1.75(2H, m), 2.32 (2H, q, J=7 Hz), 2.70 (2H, t, J=8 Hz), 3.96 (2H, s), 4.01(3H, s), 7.29-7.38 (1H, m), 7.43-7.59 (3H, m), 7.76 (1H, d, J=8 Hz),8.18 (1H, s), 8.54 (2H, s), 8.61 (1H, br s).

Example 4 Preparation of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-ethylpyrimidin-4(3H)-one

Process 1: By using 2-amino-5-ethoxypyrimidine instead of2-amino-5-methoxypyrimidine in the Process 3 of the Example 1, thereaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 80%) as a pale yellow solid.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.18 (3H, t, J=7 Hz), 1.37-1.47 (2H, m), 1.51 (3H,t, J=7 Hz), 1.62-1.72 (2H, m), 2.32 (2H, q, J=7 Hz), 2.66-2.72 (2H, m),3.97 (2H, s), 4.22 (2H, q, J=7 Hz), 7.47 (1H, t, J=8 Hz), 7.64-7.69 (2H,m), 7.74-7.83 (3H, m), 8.51 (2H, s), 8.70 (1H, d, J=2 Hz).

Process 2: By using2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-ethylpyrimidin-4(3H)-one(yield: 75%) as colorless viscous oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.18 (3H, t, J=7 Hz), 1.36-1.47 (2H, m), 1.51 (3H,t, J=7 Hz), 1.61-1.74 (2H, m), 2.33 (2H, q, J=7 Hz), 2.70 (2H, t, J=8Hz), 3.97 (2H, s), 4.22 (2H, q, J=7 Hz), 7.38 (1H, d, J=8 Hz), 7.47-7.60(3H, m), 7.78 (1H, dd, J=8, 2 Hz), 8.20-8.28 (1H, m), 8.51 (2H, s), 8.64(1H, s).

Example 5 Preparation of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-isopropyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one

Process 1: By using isobutyryl chloride instead of propionyl chloride inthe Process 1 of the Example 3, the reaction and the treatment wereperformed in the same manner as the Process 1 of the Example 3 to givemethyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-heptenoate(yield: 49%) as brown oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.90 (3H, t, J=7 Hz), 1.25 (6H, d, J=7 Hz), 1.33-1.55 (4H, m), 2.49-2.63(1H, m), 2.90-2.99 (2H, m), 3.71 (3H, s), 3.75 (2H, s), 7.49 (1H, td,J=8, 1 Hz), 7.59 (1H, dd, J=8, 2 Hz), 7.64-7.73 (2H, m), 7.79 (1H, dd,J=8, 1 Hz), 7.83 (1H, dd, J=8, 1 Hz), 8.61 (1H, d, J=1 Hz), 11.90 (1H,s).

Process 2: By using methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-heptenoateinstead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoatein the Process 3 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 1 to give2-{5-{[4-butyl-2-isopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 55%) as yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.20 (6H, d, J=7 Hz), 1.33-1.49 (2H, m), 1.62-1.75(2H, m), 2.21-2.35 (1H, m), 2.69 (2H, t, J=8 Hz), 3.95 (2H, s), 4.00(3H, s), 7.46 (1H, td, J=8, 1 Hz), 7.61-7.70 (2H, m), 7.74-7.83 (3H, m),8.53 (2H, s), 8.69 (1H, d, J=1 Hz).

Process 3: By using2-{5-{[4-butyl-2-isopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-isopropyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one(yield: 69%) as colorless viscous oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.20 (6H, d, J=7 Hz), 1.33-1.47 (2H, m), 1.60-1.75(2H, m), 2.22-2.35 (1H, m), 2.70 (2H, t, J=8 Hz), 3.95 (2H, s), 4.01(3H, s), 7.33 (1H, d, J=8 Hz), 7.45-7.57 (3H, m), 7.77 (1H, d, J=7 Hz),8.18 (1H, br s), 8.53 (2H, s), 8.61 (1H, s).

Example 6 Preparation of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-isopropylpyrimidin-4(3H)-one

Process 1: By using methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-heptenoateobtained from the Process 1 of the Example 5 instead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoatein the Process 3 of the Example 1 and also using2-amino-5-ethoxypyrimidine instead of 2-amino-5-methoxypyrimidine, thereaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 79%) as a pale yellow solid.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.19 (6H, d, J=7 Hz), 1.35-1.45 (2H, m), 1.51 (3H,t, J=7 Hz), 1.63-1.74 (2H, m), 2.22-2.35 (1H, m), 2.69 (2H, t, J=8 Hz),3.95 (2H, s), 4.22 (2H, q, J=7 Hz), 7.46 (1H, td, J=8, 1 Hz), 7.62-7.70(2H, m), 7.75-7.83 (3H, m), 8.50 (2H, s), 8.67-8.71 (1H, m).

Process 2: By using2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-isopropylpyrimidin-4(3H)-one(yield: 99%) as pale brown viscous oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.20 (6H, d, J=7 Hz), 1.35-1.46 (2H, m), 1.51 (3H,t, J=7 Hz), 1.63-1.75 (2H, m), 2.22-2.35 (1H, m), 2.71 (2H, t, J=7 Hz),3.96 (2H, s), 4.22 (2H, q, J=7 Hz), 7.37-7.45 (1H, m), 7.48-7.63 (3H,m), 7.81 (1H, dd, J=8, 2 Hz), 8.25-8.33 (1H, m), 8.51 (2H, s), 8.67 (1H,s).

Example 7 Preparation of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclopropyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one

Process 1: By using cyclopropanecarbonyl chloride instead of propionylchloride in the Process 1 of the Example 3, the reaction and thetreatment were performed in the same manner as the Process 1 of theExample 3 to give methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-(cyclopropanecarboxamide)-2-heptenoate(yield: 69%) as yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.78-0.98 (5H, m), 1.02-1.12 (2H, m), 1.31-1.65 (5H, m), 2.88-3.02 (2H,m), 3.72 (3H, s), 3.76 (2H, s), 7.50 (1H, t, J=8 Hz), 7.60 (1H, d, J=8Hz), 7.63-7.74 (2H, m), 7.76-7.87 (2H, m), 8.61 (1H, s), 12.2 (1H, s).

Process 2: By using methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-(cyclopropanecarboxamide)-2-heptenoateinstead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoatein the Process 3 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 1 to give2-{5-{[4-butyl-2-cyclopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 63%) as yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.82-0.87 (2H, m), 0.92 (3H, t, J=7 Hz), 1.07-1.15 (1H, m), 1.21-1.27(2H, m), 1.32-1.41 (2H, m), 1.53-1.64 (2H, m), 2.61 (2H, t, J=8 Hz),3.94 (2H, s), 4.01 (3H, s), 7.44-7.49 (1H, m), 7.66 (2H, t, J=8 Hz),7.74-7.82 (3H, m), 8.56 (2H, s), 8.68 (1H, d, J=2 Hz).

Process 3: By using2-{5-{[4-butyl-2-cyclopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclopropyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one(yield: 100%) as pale yellow viscous oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.82-0.89 (2H, m), 0.92 (3H, t, J=7 Hz), 1.06-1.15 (1H, m), 1.21-1.27(2H, m), 1.31-1.43 (2H, m), 1.56-1.67 (2H, m), 2.63 (2H, t, J=8 Hz),3.94 (2H, s), 4.01 (3H, s), 7.40 (1H, d, J=8 Hz), 7.47-7.62 (3H, m),7.75-7.82 (1H, m), 8.23-8.32 (1H, m), 8.56 (2H, s), 8.65 (1H, s).

Example 8 Preparation of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclobutyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one

Process 1: By using cyclobutanecarbonyl chloride instead of propionylchloride in the Process 1 of the Example 3, the reaction and thetreatment were performed in the same manner as the Process 1 of theExample 3 to give methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-(cyclobutanecarboxamide)-2-heptenoate(yield: 72%) as brown oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.91 (3H, t, J=7 Hz), 1.33-1.54 (4H, m), 2.19-2.44 (6H, m), 2.95 (2H, t,J=8 Hz), 3.12-3.25 (1H, m), 3.70 (3H, s), 3.75 (2H, s), 7.49 (1H, td,J=8, 1 Hz), 7.58 (1H, dd, J=8, 2 Hz), 7.64-7.73 (2H, m), 7.76-7.86 (2H,m), 8.60 (1H, s), 11.78 (1H, s).

Process 2: By using methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-(cyclobutanecarboxamide)-2-heptenoateinstead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoatein the Process 3 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 1 to give2-{5-{[4-butyl-2-cyclobutyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 65%) as a pale yellow solid.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.96 (3H, t, J=7 Hz), 1.34-1.51 (2H, m), 1.65-1.83 (6H, m), 2.36-2.51(2H, m), 2.71 (2H, t, J=8 Hz), 3.07-3.17 (1H, m), 3.96 (2H, s), 4.00(3H, s), 7.46 (1H, td, J=8, 1 Hz), 7.61-7.70 (2H, m), 7.73-7.82 (3H, m),8.52 (2H, s), 8.69 (1H, d, J=1 Hz).

Process 3: By using2-{5-{[4-butyl-2-cyclobutyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclobutyl-3-(5-methoxypyrimidin-2-yl)pyrimidin-4(3H)-one(yield: 74%) as colorless viscous oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.95 (3H, t, J=7 Hz), 1.34-1.50 (2H, m), 1.65-1.83 (6H, m), 2.37-2.51(2H, m), 2.72 (2H, t, J=8 Hz), 3.04-3.20 (1H, m), 3.96 (2H, s), 4.01(3H, s), 7.31 (1H, d, J=8 Hz), 7.45-7.56 (3H, m), 7.76 (1H, d, J=8 Hz),8.16 (1H, br s), 8.52 (2H, s), 8.59 (1H, s).

Example 9 Preparation of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclobutyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one

Process 1: By using methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-(cyclobutanecarboxamide)-2-heptenoateobtained from the Process 1 of the Example 8 instead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoatein the Process 3 of the Example 1 and also using2-amino-5-ethoxypyrimidine instead of 2-amino-5-methoxypyrimidine, thereaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{5-{[4-butyl-2-cyclobutyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 89%) as a pale yellow solid.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.96 (3H, t, J=7 Hz), 1.39-1.47 (2H, m), 1.51 (3H, t, J=7 Hz), 1.61-1.84(6H, m), 2.36-2.51 (2H, m), 2.67-2.75 (2H, m), 3.03-3.16 (1H, m), 3.96(2H, s), 4.22 (2H, q, J=7 Hz), 7.48 (1H, dd, J=8, 1 Hz), 7.62-7.70 (2H,m), 7.72-7.83 (3H, m), 8.49 (2H, s), 8.69 (1H, d, J=2 Hz).

Process 2: By using2-{5-{[4-butyl-2-cyclobutyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclobutyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one(yield: 99%) as pale brown viscous oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.95 (3H, t, J=7 Hz), 1.36-1.47 (2H, m), 1.51 (3H, t, J=7 Hz), 1.63-1.85(6H, m), 2.37-2.50 (2H, m), 2.73 (2H, t, J=8 Hz), 3.07-3.18 (1H, m),3.97 (2H, s), 4.22 (2H, q, J=7 Hz), 7.40 (1H, d, J=8 Hz), 7.48-7.62 (3H,m), 7.76-7.82 (1H, m), 8.24-8.31 (1H, m), 8.49 (2H, s), 8.66 (1H, s).

Example 10 Preparation of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclopentyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-2-pyrimidin-4(3H)-one

Process 1: By using cyclopentanecarbonyl chloride instead ofpropionylchloride in the Process 1 of the Example 3, the reaction andthe treatment were performed in the same manner as the Process 1 of theExample 3 to give methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-(cyclopentanecarboxamide)-2-heptenoate(yield: 44%) as brown oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.90 (3H, t, J=7 Hz), 1.33-2.03 (12H, m), 2.70-2.82 (1H, m), 2.89-2.99(2H, m), 3.71 (3H, s), 3.75 (2H, s), 7.49 (1H, td, J=8, 1 Hz), 7.59 (1H,dd, J=8, 2 Hz), 7.64-7.73 (2H, m), 7.76-7.86 (2H, m), 8.60 (1H, s),11.89 (1H, s).

Process 2: By using methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-(cyclopentanecarboxamide)-2-heptenoateinstead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoatein the Process 3 of the Example 1 and also using2-amino-5-ethoxypyrimidine instead of 2-amino-5-methoxypyrimidine, thereaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{5-{[4-butyl-2-cyclopentyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 57%) as a pale yellow solid.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.34-1.54 (7H, m), 1.60-1.80 (6H, m), 1.90-2.03(2H, m), 2.42-2.48 (1H, m), 2.64-2.70 (2H, m), 3.95 (2H, s), 4.22 (2H,q, J=7 Hz), 7.47 (1H, td, J=8, 1 Hz), 7.63-7.69 (2H, m), 7.77 (2H, dd,J=8, 1 Hz), 7.80 (1H, dd, J=8, 1 Hz), 8.51 (2H, s), 8.69 (1H, d, J=2Hz).

Process 3: By using2-{5-{[4-butyl-2-cyclopentyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclopentyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one(yield: 40%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.52 (3H, t, J=7 Hz), 1.57-1.78 (8H, m), 1.81-1.93(5H, m), 2.70 (2H, t, J=8 Hz), 3.94 (2H, s), 4.23 (2H, q, J=7 Hz), 7.38(1H, d, J=9 Hz), 7.47-7.62 (3H, m), 7.78 (1H, d, J=8 Hz), 8.22-8.29 (1H,m), 8.52 (2H, s), 8.65 (1H, s).

Example 11 Preparation of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclohexyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one

Process 1: By using cyclohexanecarbonyl chloride instead of propionylchloride in the Process 1 of the Example 3, the reaction and thetreatment were performed in the same manner as the Process 1 of theExample 3 to give methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-(cyclohexanecarboxyamide)-2-heptenoate(yield: 52%) as brown oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.90 (3H, t, J=7 Hz), 1.16-2.03 (14H, m), 2.45-2.59 (1H, m), 2.89-2.98(2H, m), 3.71 (3H, s), 3.75 (2H, s), 7.49 (2H, td, J=8, 1 Hz), 7.58 (1H,dd, J=8, 2 Hz), 7.63-7.74 (2H, m), 7.76-7.86 (2H, m), 8.61 (1H, s),11.84 (1H, br s).

Process 2: By using methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-(cyclohexanecarboxyamide)-2-heptenoateinstead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoatein the Process 3 of the Example 1 and also using 2-amino5-ethoxypyrimidine instead of 2-amino 5-methoxypyrimidine, the reactionand the treatment were performed in the same manner as the Process 3 ofthe Example 1 to give2-{5-{[4-butyl-2-cyclohexyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 80%) as a pale yellow solid.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.16-1.91 (17H, m), 2.65-2.71 (2H, m), 3.95 (2H,s), 4.23 (2H, q, J=7 Hz), 7.47 (1H, td, J=8, 1 Hz), 7.63-7.68 (2H, m),7.75-7.82 (3H, m), 8.51 (2H, s), 8.69 (1H, d, J=1 Hz).

Process 3: By using2-{5-{[4-butyl-2-cyclohexyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-cyclohexyl-3-(5-ethoxypyrimidin-2-yl)pyrimidin-4(3H)-one(yield: 58%) as colorless viscous oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.51 (3H, t, J=7 Hz), 1.61-1.82 (8H, m), 1.90-2.05(5H, m), 2.46 (2H, t, J=8 Hz), 2.69 (2H, t, J=7 Hz), 3.95 (2H, s), 4.22(2H, q, J=7 Hz), 7.39 (1H, d, J=8 Hz), 7.48-7.62 (3H, m), 7.79 (1H, dd,J=8, 2 Hz), 8.22-8.31 (1H, m), 8.51 (2H, s), 8.65 (1H, s).

Example 12 Preparation of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-methyl-3-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}pyrimidin-4(3H)-one

Process 1: By using 2-amino-5-[2-(methylthio)ethoxy]pyrimidine insteadof 2-amino-5-methoxypyrimidine in the Process 3 of the Example 1, thereaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}benzonitrile(yield: 64%) as yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.95 (3H, t, J=7 Hz), 1.33-1.48 (2H, m), 1.57-1.73 (2H, m), 2.17 (3H,s), 2.24 (3H, s), 2.67 (2H, t, J=8 Hz), 2.96 (2H, t, J=7 Hz), 3.97 (2H,s), 4.33 (2H, t, J=7 Hz), 7.47 (1H, t, J=8 Hz), 7.62-7.70 (2H, m),7.73-7.83 (3H, m), 8.55 (2H, s), 8.70 (1H, s).

Process 2: By using2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-methyl-3-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}pyrimidin-4(3H)-one(yield: 80%) as yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.82-1.00 (3H, m), 1.33-1.47 (2H, m), 1.55-1.73 (2H, m), 2.15 (3H, s),2.23 (3H, s), 2.55-2.76 (2H, m), 2.95 (2H, t, J=7 Hz), 3.82-4.03 (2H,m), 4.33 (2H, t, J=7 Hz), 7.07-7.33 (1H, m), 7.35-7.57 (3H, m),7.59-7.80 (1H, m), 7.85-8.15 (1H, m), 8.47-8.62 (1H, m), 8.55 (2H, s).

Example 13 Preparation of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-methyl-3-{5-[2-(methylsulfonyl)ethoxy]pyrimidin-2-yl}pyrimidin-4(3H)-one

Methanol 0.4 mL) solution of hydrogen peroxide (30% solution, 24 mg,0.211 mmol) and methanol (0.4 mL) solution of tantalum chloride (1.5 mg,0.0042 mmol) were added to methanol (1.0 mL) solution of5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-methyl-3-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}pyrimidin-4(3H)-one(24 mg, 0.042 mmol) which has been obtained in the Example 12. Afterstirring for 12 hours at room temperature, the solvent was removed bydistillation. The obtained residues were subjected to silica gel columnchromatography (chloroform:methanol:triethylamine=4:1:0.4) to give5-{{6-[2-(1H-tetrazol-5-yl)phenyl]pyridin-3-yl}methyl}-6-butyl-2-methyl-3-{5-[2-(methylsulfonyl)ethoxy]pyrimidin-2-yl}pyrimidin-4(3H)-one(24 mg, 93%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.34-1.47 (2H, m), 1.54-1.71 (2H, m), 2.16 (3H,s), 2.66 (2H, t, J=8 Hz), 3.09 (3H, s), 3.55 (2H, t, J=5 Hz), 3.93 (2H,s), 4.64 (2H, t, J=5 Hz), 7.10-7.24 (1H, m), 7.31-7.55 (3H, m),7.65-7.77 (1H, m), 7.92-8.04 (1H, m), 8.45-8.53 (1H, m), 8.59 (2H, s).

Example 14 Preparation of3-{2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using 2-amino-pyridine instead of2-amino-5-methoxypyrimidine in the Process 3 of the Example 1, thereaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 61%).

¹H-NMR (CDCl₃, 400 MHz) δ:

0.95 (3H, t, J=7 Hz), 1.43 (2H, sextet, J=8 Hz), 1.61-1.69 (2H, m), 2.17(3H, s), 2.66-2.70 (2H, m), 3.97 (2H, s), 7.36-7.50 (3H, m), 7.65-7.69(2H, m), 7.76-7.81 (3H, m), 7.93 (1H, m), 8.67-8.70 (2H, m).

Process 2: Sodium hydrogen carbonate (2.02 mg, 24.0 mmol) was added todimethyl sulfoxide solution (20 mL) of hydroxylamine hydrochloride (1.42g, 20.4 mmol) and stirred for 1 hour at 40° C. Dimethyl sulfoxidesolution (3 mL) of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(430 mg, 0.987 mmol) was added to the reaction mixture and stirred for19 hours at 90° C. The reaction mixture was added water and extractedwith ethyl acetate. The organic layer was combined, washed with waterand brine, dried over anhydrous sodium sulfate, and concentrated invacuo. The obtained residues were subjected to silica gel columnchromatography (ethyl acetate) to give2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide(430 mg, 93%) as a white solid.

Process 3: 1,1′-Carbonyldiimidazole (490 mg, 3.02 mmol) and1,8-diazabicyclo[5.4.0]undec-7-ene (460 mg, 3.02 mmol) were added todimethylformamide solution (25 mL) of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide(430 mg, 0.918 mmol) and stirred for 3 hours at room temperature. Oncethe reaction is completed, the reaction mixture was added water andextracted with ethyl acetate. The organic layer was combined, washedwith water and brine, dried over anhydrous sodium sulfate, andconcentrated in vacuo. The obtained residues were purified by silica gelcolumn chromatography (ethyl acetate) to give3-{2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(160 mg, 35%, two step yield) as weak yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.42 (2H, sextet, J=8 Hz), 1.60-1.68 (2H, m), 2.17(3H, s), 2.64-2.68 (2H, m), 3.93 (2H, s), 7.33-7.56 (6H, m), 7.74-7.77(2H, m), 7.95 (1H, dd, J=8, 2 Hz), 8.45 (1H, s), 8.67 (1H, d, J=4 Hz).

Example 15 Preparation of3-{2-{5-{[4-butyl-2-methyl-1-(4-methylpyridin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using 2-amino-4-methylpyridine instead of2-amino-5-methoxypyrimidine in the Process 3 of the Example 1, thereaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{5-{[4-butyl-2-methyl-1-(4-methylpyridin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 61%).

¹H-NMR (CDCl₃, 400 MHz) δ:

0.95 (3H, t, J=7 Hz), 1.42 (2H, sextet, J=8 Hz), 1.60-1.69 (2H, m), 2.17(3H, s), 2.45 (3H, s), 2.66-2.70 (2H, m), 3.96 (2H, s), 7.19 (1H, s),7.24-7.27 (2H, m), 7.48 (1H, m), 7.65-7.69 (2H, m), 7.76-7.82 (2H, m),8.51 (1H, d, J=5 Hz), 8.70 (1H, s).

Process 2: By using2-{5-{[4-butyl-2-methyl-1-(4-methylpyridin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{[4-butyl-2-methyl-1-(4-methylpyridin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide.

Process 3: By using2-{5-{[4-butyl-2-methyl-1-(4-methylpyridin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{[4-butyl-2-methyl-1-(4-methylpyridin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 45%, two step yield) as weak yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.95 (3H, t, J=7 Hz), 1.42 (2H, sextet, J=8 Hz), 1.61-1.69 (2H, m), 2.17(3H, s), 2.46 (3H, s), 2.65-2.69 (2H, m), 3.94 (2H, s), 7.21 (1H, s),7.24-7.28 (2H, m), 7.37-7.60 (3H, m), 7.78 (1H, dd, J=8, 2 Hz), 7.85(1H, d, J=7 Hz), 8.50-8.51 (2H, m).

Example 16 Preparation of3-{2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileobtained from the Process 3 of the Example 1 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide.

Process 2: By using2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 48%, two step yield) as colorless amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.43 (2H, quint, J=8 Hz), 1.61-1.68 (2H, m), 2.17(3H, s), 2.65-2.69 (2H, m), 3.95 (2H, s), 4.01 (3H, s), 7.36-7.69 (4H,m), 7.76-7.86 (2H, m), 8.51 (1H, br), 8.54 (2H, s).

Example 17 Preparation of3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileobtained from the Process 1 of the Example 2 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide.

Process 2: By using2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 18%, two step yield) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.95 (3H, t, J=7 Hz), 1.38-1.48 (2H, m), 1.51 (3H, t, J=7 Hz), 1.62-1.68(2H, m), 2.17 (3H, s), 2.66-2.70 (2H, m), 3.95 (2H, s), 4.22 (2H, q, J=7Hz), 7.38-7.61 (4H, m), 7.79 (1H, d, J=7 Hz), 7.90 (1H, d, J=7 Hz), 8.51(2H, s), 8.54 (1H, s).

Example 18 Preparation of3-{2-{5-{[4-butyl-2-ethyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{5-{[4-butyl-2-ethyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileobtained from the Process 2 of the Example 3 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{[4-butyl-2-ethyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide.

Process 2: By using2-{5-{[4-butyl-2-ethyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{[4-butyl-2-ethyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 53%, two step yield) as white amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.95 (3H, t, J=7 Hz), 1.18 (3H, t, J=7 Hz), 1.36-1.50 (2H, m), 1.61-1.75(2H, m), 2.32 (2H, q, J=7 Hz), 2.71 (2H, t, J=8 Hz), 3.95 (2H, s), 4.00(3H, s), 4.79 (1H, br s), 7.38 (1H, d, J=8 Hz), 7.45 (1H, dd, J=8, 1Hz), 7.51 (1H, dd, J=8, 1 Hz), 7.59 (1H, td, J=8, 2 Hz), 7.79 (1H, dd,J=8, 2 Hz), 7.89 (1H, dd, J=8, 1 Hz), 8.52-8.55 (3H, m).

Example 19 Preparation of3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileobtained from the Process 1 of the Example 4 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide.

Process 2: By using2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 73%, two step yield) as white amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.18 (3H, t, J=7 Hz), 1.34-1.47 (2H, m), 1.51 (3H,t, J=7 Hz), 1.60-1.74 (2H, m), 2.32 (2H, q, J=7 Hz), 2.70 (2H, t, J=8Hz), 3.94 (2H, s), 4.22 (2H, q, J=7 Hz), 7.36 (1H, d, J=8 Hz), 7.41-7.61(3H, m), 7.77 (1H, dd, J=8, 2 Hz), 7.85 (1H, dd, J=8, 1 Hz), 8.48-8.53(3H, m).

Example 20 Preparation of3-{2-{5-{[4-butyl-2-isopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{5-{[4-butyl-2-isopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileobtained from the Process 2 of the Example 5 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{[4-butyl-2-isopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide.

Process 2: By using2-{5-{[4-butyl-2-isopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{[4-butyl-2-isopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 60%, two step yield) as white amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.95 (3H, t, J=7 Hz), 1.19 (6H, d, J=7 Hz), 1.31-1.49 (2H, m), 1.60-1.75(2H, m), 2.23-2.35 (1H, m), 2.70 (2H, t, J=8 Hz), 3.93 (2H, s), 4.00(3H, s), 7.36 (1H, d, J=8 Hz), 7.43 (1H, dd, J=7, 1 Hz), 7.49 (1H, dd,J=7, 1 Hz), 7.57 (1H, td, J=8, 1 Hz), 7.79 (1H, dd, J=8, 2 Hz), 7.85(1H, dd, J=8, 1 Hz), 8.50 (1H, d, J=2 Hz), 8.53 (2H, s).

Example 21 Preparation of3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileobtained from the Process 1 of the Example 6 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide.

Process 2: By using2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 66%, two step yield) as white amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.95 (3H, t, J=7 Hz), 1.20 (6H, d, J=7 Hz), 1.36-1.46 (2H, m), 1.51 (3H,t, J=7 Hz), 1.62-1.74 (2H, m), 2.23-2.35 (1H, m), 2.72 (2H, t, J=8 Hz),3.94 (2H, s), 4.22 (2H, q, J=7 Hz), 7.40 (1H, d, J=9 Hz), 7.46 (1H, dd,J=8, 1 Hz), 7.52 (1H, td, J=8, 2 Hz), 7.61 (1H, td, J=8, 2 Hz), 7.82(1H, dd, J=8, 2 Hz), 7.95 (1H, dd, J=8, 1 Hz), 8.51 (2H, s), 8.58 (1H,d, J=2 Hz).

Example 22 Preparation of3-{2-{5-{[4-butyl-2-cyclopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{5-{[4-butyl-2-cyclopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileobtained from the Process 2 of the Example 7 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{[4-butyl-2-cyclopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide.

Process 2: By using2-{5-{[4-butyl-2-cyclopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{[4-butyl-2-cyclopropyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 84%, two step yield) as white amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.81-0.89 (2H, m), 0.93 (3H, t, J=7 Hz), 1.06-1.15 (1H, m), 1.24 (2H, t,J=4 Hz), 1.32-1.44 (2H, m), 1.55-1.67 (2H, m), 2.63 (2H, t, J=8 Hz),3.92 (2H, s), 4.00 (3H, s), 7.37 (1H, d, J=8 Hz), 7.45 (1H, d, J=8 Hz),7.51 (1H, dd, J=8, 1 Hz), 7.59 (1H, td, J=8, 1 Hz), 7.78 (1H, dd, J=8, 2Hz), 7.89 (1H, d, J=7 Hz), 8.52 (1H, d, J=2 Hz), 8.56 (2H, s).

Example 23 Preparation of3-{2-{5-{[4-butyl-2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using 2-amino-5-ethoxypyrimidine instead of2-amino-5-methoxypyrimidine in the Process 3 of the Example 1 and alsousing methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-(cyclopropanecarboxamide)-2-heptenoateinstead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoate,the reaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{5-{[4-butyl-2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 65%) as yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.79-0.87 (2H, m), 0.92 (3H, t, J=8 Hz), 1.09-1.16 (1H, m), 1.18-1.29(2H, m), 1.30-1.43 (2H, m), 1.51 (3H, t, J=7 Hz), 1.54-1.66 (2H, m),2.61 (2H, t, J=8 Hz), 3.94 (2H, s), 4.22 (2H, q, J=7 Hz), 7.47 (1H, t,J=8 Hz), 7.57-7.69 (2H, m), 7.71-7.83 (3H, m), 8.54 (2H, s), 8.68 (1H,s).

Process 2: By using2-{5-{[4-butyl-2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{[4-butyl-2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide.

Process 3: By using2-{5-{[4-butyl-2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{[4-butyl-2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 38%, two step yield) as colorless crystalline powder.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.76-0.87 (2H, m), 0.92 (3H, t, J=7 Hz), 1.05-1.15 (1H, m), 1.16-1.28(2H, m), 1.32-1.44 (2H, m), 1.51 (3H, t, J=7 Hz), 1.54-1.66 (2H, m),2.61 (2H, t, J=8 Hz), 3.91 (2H, s), 4.22 (2H, q, J=7 Hz), 7.34 (1H, d,J=8 Hz), 7.38-7.50 (2H, m), 7.51-7.59 (1H, m), 7.71-7.86 (2H, m), 8.46(1H, s), 8.54 (2H, s).

Example 24 Preparation of3-{2-{5-{[4-butyl-2-cyclobutyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{5-{[4-butyl-2-cyclobutyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileobtained from the Process 2 of the Example 8 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{[4-butyl-2-cyclobutyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxbenzimidamide.

Process 2: By using2-{5-{[4-butyl-2-cyclobutyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxbenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{[4-butyl-2-cyclobutyl-1-(5-methoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 65%, two step yield) as white amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.96 (3H, t, J=7 Hz), 1.35-1.51 (2H, m), 1.64-1.85 (6H, m), 2.37-2.53(2H, m), 2.72 (2H, t, J=8 Hz), 3.04-3.20 (1H, m), 3.94 (2H, s), 4.00(3H, s), 7.34 (1H, d, J=8 Hz), 7.39-7.44 (1H, m), 7.44-7.49 (1H, m),7.51-7.59 (1H, m), 7.74-7.83 (2H, m), 8.48 (1H, d, J=2 Hz), 8.52 (2H,s).

Example 25 Preparation of3-{2-{5-{[4-butyl-2-cyclobutyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{5-{[4-butyl-2-cyclobutyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileobtained from the Process 1 of the Example 9 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{[4-butyl-2-cyclobutyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide.

Process 2: By using2-{5-{[4-butyl-2-cyclobutyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{[4-butyl-2-cyclobutyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 48%, two step yield) as white amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.97 (3H, t, J=7 Hz), 1.35-1.47 (2H, m), 1.48-1.83 (9H, m), 2.38-2.52(2H, m), 2.74 (2H, t, J=8 Hz), 3.03-3.18 (1H, m), 3.95 (2H, s), 4.22(2H, q, J=7 Hz), 7.40 (1H, d, J=8 Hz), 7.46 (1H, d, J=8 Hz), 7.54 (1H,dd, J=8, 2 Hz), 7.61 (1H, td, J=8, 2 Hz), 7.81 (1H, dd, J=8, 2 Hz), 7.95(1H, dd, J=8, 1 Hz), 8.49 (2H, s), 8.58 (1H, d, J=2 Hz).

Example 26 Preparation of3-{2-{5-{[4-butyl-2-cyclopentyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{5-{[4-butyl-2-cyclopentyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileobtained from the Process 2 of the Example 10 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{[4-butyl-2-cyclopentyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxbenzimidamide.

Process 2: By using2-{5-{[4-butyl-2-cyclopentyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxbenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{[4-butyl-2-cyclopentyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 56%, two step yield) as pale brown amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.32-1.57 (7H, m), 1.60-1.85 (6H, m), 1.90-2.06(2H, m), 2.36-2.52 (1H, m), 2.68 (2H, t, J=7 Hz), 3.93 (2H, s), 4.22(2H, q, J=7 Hz), 7.35 (1H, d, J=8 Hz), 7.40-7.60 (3H, m), 7.78 (1H, dd,J=8, 2 Hz), 7.83 (1H, dd, J=8, 1 Hz), 8.49 (1H, d, J=2 Hz), 8.51 (2H,s).

Example 27 Preparation of3-{2-{5-{[4-butyl-2-cyclohexyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{5-{[4-butyl-2-cyclohexyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileobtained from the Process 2 of the Example 11 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{[4-butyl-2-cyclohexyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide.

Process 2: By using2-{5-{[4-butyl-2-cyclohexyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{[4-butyl-2-cyclohexyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 60%) as pale brown amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.89-1.07 (5H, m), 1.34-1.94 (16H, m), 2.68 (2H, t, J=8 Hz), 3.92 (2H,s), 4.23 (2H, q, J=7 Hz), 7.34 (1H, d, J=8 Hz), 7.39-7.49 (2H, m),7.50-7.59 (1H, m), 7.74-7.83 (2H, m), 8.47 (1H, d, J=2 Hz), 8.51 (2H,s).

Example 28 Preparation of3-{2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}benzonitrileobtained from the Process 1 of the Example 12 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}-N′-hydroxybenzimidamide.

Process 2: By using2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 56%, two step yield) as weak yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.95 (3H, t, J=7 Hz), 1.40-1.46 (2H, m), 1.50-1.70 (2H, m), 2.17 (3H,s), 2.24 (3H, s), 2.68-2.71 (2H, m), 2.96 (2H, t, J=7 Hz), 3.96 (2H, s),4.33 (2H, t, J=7 Hz), 7.40-7.62 (4H, m), 7.66-7.97 (2H, m), 8.55 (2H,s), 8.58 (1H, s).

Example 29 Preparation of3-{2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylsulfonyl)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

By using3-{2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylthio)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-oneobtained in the Example 28, the reaction and the treatment wereperformed in the same manner as the Example 13 to give3-{2-{5-{{4-butyl-2-methyl-1-{5-[2-(methylsulfonyl)ethoxy]pyrimidin-2-yl}-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 63%) as colorless oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.95 (3H, t, J=7 Hz), 1.40-1.46 (2H, m), 1.65-1.70 (2H, m), 2.18 (3H,s), 2.67-2.71 (2H, m), 3.09 (3H, s), 3.53-3.55 (2H, m), 3.92 (2H, s),4.63-4.66 (2H, m), 7.36-7.60 (4H, m), 7.74 (1H, d, J=8 Hz), 7.88 (1H, d,J=8 Hz), 8.59 (1H, s), 8.60 (2H, s).

Example 30 Preparation of5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-2-methyl-3-(pyridin-2-yl)pyrimidin-4(3H)-one

Process 1: By using 2-[6-(bromomethyl)pyridin-3-yl]benzonitrile insteadof 2-[5-(bromomethyl)pyridin-2-yl]benzonitrile in the Process 1 of theExample 1, the reaction and the treatment were performed in the samemanner as the Process 1 of the Example 1 to give2-{[5-(2-cyanophenyl)pyridin-2-yl]methyl}-3-oxoheptanoate (yield: 69%)as yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.89 (3H, t, J=7 Hz), 1.24-1.34 (2H, m), 1.54-1.61 (2H, m), 2.59-2.76(2H, m), 3.37-3.55 (2H, m), 3.73 (3H, s), 4.37 (1H, t, J=7 Hz), 7.33(1H, d, J=8 Hz), 7.50 (2H, t, J=7 Hz), 7.66-7.70 (1H, m), 7.78-7.83 (2H,m), 8.63 (1H, d, J=2 Hz).

Process 2: By using methyl2-{[5-(2-cyanophenyl)pyridin-2-yl]methyl}-3-oxoheptanoate instead ofmethyl 2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxoheptanoate in theProcess 2 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 1 to givemethyl(Z)-3-acetamide-2-{[5-(2-cyanophenyl)pyridin-2-yl]methyl}-2-heptenoate(yield: 100%) as yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.89 (3H, t, J=7 Hz), 1.27-1.40 (2H, m), 1.47-1.59 (2H, m), 2.24 (3H,s), 3.14 (2H, t, J=8 Hz), 3.78 (3H, s), 3.88 (2H, s), 7.42-7.56 (3H, m),7.65-7.91 (3H, m), 8.63 (1H, s), 10.9 (1H, s).

Process 3: By using 2-aminopyridine instead of2-amino-5-methoxypyrimidine in the Process 3 of the Example 1 and alsousing methyl(Z)-3-acetamide-2-{[5-(2-cyanophenyl)pyridin-2-yl]methyl}-2-heptenoateinstead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoate,the reaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{6-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrile(yield: 35%).

¹H-NMR (CDCl₃, 400 MHz) δ:

0.93 (3H, t, J=7 Hz), 1.42 (2H, sextet, J=8 Hz), 1.60-1.75 (2H, m), 2.17(3H, s), 2.74-2.78 (2H, m), 4.17 (2H, s), 7.38-7.50 (5H, m), 7.67 (1H,m), 7.77-7.80 (2H, m), 7.93 (1H, m), 8.65 (1H, d, J=2 Hz), 8.68 (1H, d,J=3 Hz).

Process 4: By using2-{6-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-2-methyl-3-(pyridin-2-yl)pyrimidin-4(3H)-one(yield: 79%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.89 (3H, t, J=7 Hz), 1.30-1.35 (2H, m), 1.50-1.58 (2H, m), 2.18 (3H,s), 2.51-2.54 (2H, m), 3.75 (2H, s), 6.99 (1H, d, J=8 Hz), 7.16 (1H, d,J=8 Hz), 7.31-7.36 (3H, m), 7.48-7.56 (2H, m), 7.83-7.87 (2H, m), 7.97(1H, s), 8.56 (1H, d, J=4 Hz).

Example 31 Preparation of5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(5-methoxypyridin-2-yl)-2-methylpyrimidin-4(3H)-one

Process 1: By using 2-amino-5-methoxypyridine instead of2-amino-5-methoxypyrimidine in the Process 3 of the Example 1 and alsousing methyl(Z)-3-acetamide-2-{[5-(2-cyanophenyl)pyridin-2-yl]methyl}-2-heptenoateobtained from the Process 2 of the Example 30 instead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoate,the reaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{6-{[4-butyl-1-(5-methoxypyridin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrile(yield: 65%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.93 (3H, t, J=7 Hz), 1.37-1.46 (2H, m), 1.58-1.66 (2H, m), 2.18 (3H,s), 2.76 (2H, t, J=8 Hz), 3.92 (3H, s), 4.16 (2H, s), 7.27-7.30 (1H, m),7.38-7.49 (4H, m), 7.65-7.69 (1H, m), 7.77-7.79 (2H, m), 8.30 (1H, d,J=3 Hz), 8.65 (1H, d, J=2 Hz).

Process 2: By using2-{6-{[4-butyl-1-(5-methoxypyridin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(5-methoxypyridin-2-yl)-2-methylpyrimidin-4(3H)-one(yield: 72%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.87 (3H, t, J=7 Hz), 1.21-1.30 (2H, m), 1.40-1.48 (2H, m), 2.09 (3H,s), 2.38 (2H, t, J=8 Hz), 3.60 (2H, s), 3.90 (3H, s), 7.00 (1H, d, J=8Hz), 7.14 (2H, dd, J=8, 2 Hz), 7.20 (1H, d, J=9 Hz), 7.34-7.38 (2H, m),7.53-7.61 (2H, m), 7.84 (1H, d, J=7 Hz), 7.90 (1H, s), 8.21 (1H, d, J=3Hz).

Example 32 Preparation of5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]-2-methylpyrimidin-4(3H)-one

Process 1: By using 2-amino-3-chloro-5-(trifluoromethyl)pyridine insteadof 2-amino-5-methoxypyrimidine in the Process 3 of the Example 1 andalso using methyl(Z)-3-acetamide-2-{[5-(2-cyanophenyl)pyridin-2-yl]methyl}-2-heptenoateobtained from the Process 2 of the Example 30 instead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoate,the reaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{6-{{4-butyl-1-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-3-yl}benzonitrile(yield: 41%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.94 (3H, t, J=7 Hz), 1.37-1.47 (2H, m), 1.57-1.68 (2H, m), 2.16 (3H,s), 2.70-2.83 (2H, m), 4.19 (2H, s), 7.38 (1H, d, J=8 Hz), 7.46-7.53(2H, m), 7.65-7.69 (1H, m), 7.77-7.83 (2H, m), 7.89 (1H, m), 8.65 (1H,d, J=2 Hz), 8.84 (1H, s).

Process 2: By using2-{6-{{4-butyl-1-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl}methyl}pyridin-3-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]-2-methylpyrimidin-4(3H)-one(yield: 43%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.87 (3H, t, J=7 Hz), 1.22-1.30 (2H, m), 1.43-1.50 (2H, m), 2.09 (3H,s), 2.35-2.43 (2H, m), 3.55 (2H, dd, J=19, 16 Hz), 6.95 (1H, d, J=8 Hz),7.11-7.14 (1H, m), 7.38-7.40 (1H, m), 7.54-7.61 (2H, m), 7.86-7.89 (1H,m), 7.94 (1H, m), 8.18 (1H, d, J=2 Hz), 8.81 (1H, s).

Example 33 Preparation on5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(5-methoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one

Process 1: By using methyl(Z)-3-acetamide-2-{[5-(2-cyanophenyl)pyridin-2-yl]methyl}-2-heptenoateobtained from the Process 2 of the Example 30 instead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoatein the Process 3 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 1 to give2-{6-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrile(yield: 51%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.93 (3H, t, J=7 Hz), 1.36-1.45 (2H, m), 1.57-1.65 (2H, m), 2.16 (3H,s), 2.75 (2H, t, J=8 Hz), 4.00 (3H, s), 4.17 (2H, s), 7.40-7.49 (3H, m),7.64-7.69 (1H, m), 7.77-7.79 (2H, m), 8.54 (2H, s), 8.65 (1H, d, J=2Hz).

Process 2: By using2-{6-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(5-methoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one(yield: 52%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.86 (3H, t, J=7 Hz), 1.20-1.29 (2H, m), 1.41-1.49 (2H, m), 2.09 (3H,s), 2.43 (2H, t, J=8 Hz), 3.62 (2H, s), 3.98 (3H, s), 7.00 (1H, d, J=8Hz), 7.13 (1H, dd, J=8, 2 Hz), 7.39 (1H, d, J=8 Hz), 7.51-7.60 (2H, m),7.84 (1H, d, J=8 Hz), 7.95 (1H, d, J=2 Hz), 8.48 (2H, s).

Example 34 Preparation of5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one

Process 1: By using 2-amino-5-ethoxypyrimidine instead of2-amino-5-methoxypyrimidine in the Process 3 of the Example 1 and alsousing methyl(Z)-3-acetamide-2-{[5-(2-cyanophenyl)pyridin-2-yl]methyl}-2-heptenoateobtained from the Process 2 of the Example 30 instead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoate,the reaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{6-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrile(yield: 70%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.92 (3H, t, J=7 Hz), 1.36-1.45 (2H, m), 1.51 (3H, t, J=7 Hz), 1.57-1.65(2H, m), 2.16 (3H, s), 2.75 (2H, t, J=8 Hz), 4.18 (2H, s), 4.22 (2H, q,J=7 Hz), 7.41-7.52 (3H, m), 7.64-7.68 (1H, m), 7.77-7.81 (2H, m), 8.52(2H, s), 8.63-8.65 (1H, m).

Process 2: By using2-{6-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(5-ethoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one(yield: 63%) as yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.86 (3H, t, J=7 Hz), 1.18-1.29 (2H, m), 1.40-1.50 (2H, m), 1.49 (3H, t,J=7 Hz), 2.09 (3H, s), 2.42 (2H, t, J=8 Hz), 3.61 (2H, s), 4.20 (q, 2H,J=7 Hz), 7.00 (1H, d, J=8 Hz), 7.12 (1H, dd, J=8, 2 Hz), 7.39 (1H, d,J=8 Hz), 7.51-7.61 (2H, m), 7.86 (1H, d, J=7 Hz), 7.74 (1H, d, J=2 Hz),8.46 (2H, s).

Example 35 Preparation of5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(4,6-dimethoxypyrimidin-2-methylpyrimidin-4(3H)-one

Process 1: By using 2-amino-4,6-dimethoxypyrimidine instead of2-amino-5-methoxypyrimidine in the Process 3 of the Example 1 and alsousing methyl(Z)-3-acetamide-2-{[5-(2-cyanophenyl)pyridin-2-yl]methyl}-2-heptenoateobtained from the Process 2 of the Example 30 instead of methyl(Z)-3-acetamide-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-heptenoate,the reaction and the treatment were performed in the same manner as theProcess 3 of the Example 1 to give2-{6-{[4-butyl-1-(4,6-dimethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrile(yield: 49%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.93 (3H, t, J=7 Hz), 1.38-1.47 (2H, m), 1.56-1.67 (2H, m), 2.24 (3H,s), 2.76 (2H, t, J=8 Hz), 3.96 (6H, s), 4.19 (2H, s), 6.12 (1H, s),7.45-7.50 (3H, m), 7.65-7.69 (1H, m), 7.77-7.82 (2H, m), 8.66 (1H, d,J=2 Hz).

Process 2: By using2-{6-{[4-butyl-1-(4,6-dimethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrileinstead of2-{5-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 4 of the Example 1, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 1 to give5-{{5-[2-(1H-tetrazol-5-yl)phenyl]pyridin-2-yl}methyl}-6-butyl-3-(4,6-dimethoxypyrimidin-2-yl)-2-methylpyrimidin-4(3H)-one(yield: 53%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.88 (3H, t, J=7 Hz), 1.22-1.32 (2H, m), 1.43-1.50 (2H, m), 2.17 (3H,s), 2.42 (2H, t, J=8 Hz), 3.62 (2H, s), 3.89 (6H, s), 6.06 (1H, s), 7.02(1H, d, J=8 Hz), 7.14 (1H, dd, J=8, 2 Hz), 7.40 (1H, d, J=8 Hz),7.53-7.62 (2H, m), 7.31 (1H, d, J=8 Hz), 7.95 (1H, s).

Example 36 Preparation on3-{2-{6-{[4-butyl-1-(5-methoxypyridin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{6-{[4-butyl-1-(5-methoxypyridin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrileobtained from the Process 1 of the Example 31 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{6-{[4-butyl-1-(5-methoxypyridin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}-N′-hydroxybenzimidamide(yield: 64%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.90 (3H, t, J=7 Hz), 1.34-1.43 (2H, m), 1.54-1.62 (2H, m), 2.16 (3H,s), 2.71 (2H, t, J=8 Hz), 3.91 (3H, s), 4.13 (2H, s), 4.50 (2H, s),7.29-7.42 (5H, m), 7.45-7.49 (1H, m), 7.55-7.57 (1H, m), 7.66-7.69 (1H,m), 8.29 (1H, d, J=3 Hz), 8.60 (1H, d, J=2 Hz).

Process 2: By using2-{6-{[4-butyl-1-(5-methoxypyridin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{6-{[4-butyl-1-(5-methoxypyridin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 70%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.92 (3H, t, J=7 Hz), 1.30-1.39 (2H, m), 1.49-1.57 (2H, m), 2.11 (3H,s), 2.51 (2H, t, J=8 Hz), 3.62 (2H, s), 3.91 (3H, s), 7.15 (1H, d, J=8Hz), 7.23 (2H, d, J=9 Hz), 7.32-7.39 (2H, m), 7.48-7.52 (2H, m),7.57-7.61 (1H, m), 7.70 (1H, d, J=8 Hz), 7.99 (1H, s), 8.18 (1H, d, J=3Hz).

Example 37 Preparation of3-{2-{6-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{6-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrileobtained from the Process 1 of the Example 33 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{6-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}-N′-hydroxybenzimidamide(yield: 50%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.90 (3H, t, J=7 Hz), 1.34-1.43 (2H, m), 1.54-1.62 (2H, m), 2.15 (3H,s), 2.73 (2H, t, J=8 Hz), 3.99 (3H, s), 4.13 (2H, s), 4.50 (2H, s),7.28-7.42 (3H, m), 7.45-7.49 (1H, m), 7.53-7.57 (1H, m), 7.66-7.69 (1H,m), 8.53 (2H, s), 8.59 (1H, d, J=2 Hz).

Process 2: By using2-{6-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{6-{[4-butyl-1-(5-methoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 85%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.90 (3H, t, J=7 Hz), 1.27-1.36 (2H, m), 1.45-1.53 (2H, m), 2.11 (3H,s), 2.45 (2H, t, J=8 Hz), 3.56 (2H, s), 4.00 (3H, s), 7.12 (1H, d, J=8Hz), 7.38 (1H, d, J=8 Hz), 7.50-7.60 (2H, m), 7.60-7.64 (1H, m), 7.72(1H, d, J=1 Hz), 7.90 (1H, s), 8.51 (2H, s).

Example 38 Preparation of3-{2-{6-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{6-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrileobtained from the Process 1 of the Example 34 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{6-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}-N′-hydroxybenzimidamide(yield: 52%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.90 (3H, t, J=7 Hz), 1.35-1.43 (2H, m), 1.50 (3H, t, J=7 Hz), 1.51-1.62(2H, m), 2.15 (3H, s), 2.72 (2H, t, J=8 Hz), 4.13 (2H, s), 4.21 (2H, q,J=7 Hz), 4.51 (2H, s), 7.28-7.49(4H, m), 7.55-7.57 (1H, m), 7.66-7.69(1H, m), 8.50 (2H, s), 8.59-8.60 (1H, m).

Process 2: By using2-{6-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{6-{[4-butyl-1-(5-ethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 89%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.90 (3H, t, J=7 Hz), 1.27-1.36 (2H, m), 1.45-1.52 (5H, m), 2.11 (3H,s), 2.49 (2H, t, J=8 Hz), 3.59 (2H, s), 4.22 (2H, q, J=7 Hz), 7.18 (1H,d, J=8 Hz), 7.38 (1H, d, J=8 Hz), 7.50-7.55 (2H, m), 7.60-7.64 (1H, m),7.72 (1H, d, J=8 Hz), 7.93-7.97 (1H, m), 8.49 (2H, s).

Example 39 Preparation of3-{2-{6-{[4-butyl-1-(4,6-dimethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using2-{6-{[4-butyl-1-(4,6-dimethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}benzonitrilein the Process 1 of the Example 35 instead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 2 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 14 to give2-{6-{[4-butyl-1-(4,6-dimethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}-N′-hydroxybenzimidamide(yield: 47%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.92 (3H, t, J=7 Hz), 1.36-1.45 (2H, m), 1.56-1.64 (2H, m), 2.23 (3H,s), 2.73 (2H, t, J=8 Hz), 3.95 (6H, s), 4.14 (2H, s), 4.49 (2H, s), 6.12(1H, s), 7.32-7.43 (3H, m), 7.46-7.50 (1H, m), 7.56-7.58 (1H, m),7.69-7.71 (1H, m), 8.57-8.61 (1H, m).

Process 2: By using2-{6-{[4-butyl-1-(4,6-dimethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[4-butyl-2-methyl-6-oxo-1-(pyridin-2-yl)-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 3 of the Example 14, the reaction and the treatment wereperformed in the same manner as the Process 3 of the Example 14 to give3-{2-{6-{[4-butyl-1-(4,6-dimethoxypyrimidin-2-yl)-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-3-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 52%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.92 (3H, t, J=7 Hz), 1.31-1.40 (2H, m), 1.50-1.58 (2H, m), 2.18 (3H,s), 2.51 (2H, t, J=8 Hz), 3.67 (2H, s), 3.92 (6H, s), 6.08 (1H, s), 7.21(1H, d, J=8 Hz), 7.41 (1H, d, J=8 Hz), 7.50-7.56 (2H, m), 7.63 (1H, t,J=8 Hz), 7.74 (1H, d, J=8 Hz), 8.01 (1H, d, J=2 Hz).

Example 40 Preparation of3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: Under argon atmosphere, tetrahydrofuran (20 mL) mixturecontaining 2-[5-(bromomethyl)pyridin-2-yl]benzonitrile (1.1 g, 3.9mmol), methyl 3-oxohexanoate (0.68 g, 4.7 mmol), diisopropylethylamine(1.0 g, 7.8 mmol), and lithium bromide monohydrate (0.49 g, 4.7 mmol)was refluxed under heating for 18 hours. The reaction mixture was addedwater and extracted three times with chloroform. The organic layer wascombined, washed with water and brine, dried over anhydrous sodiumsulfate, and concentrated in vacuo. The obtained residues were subjectedto silica gel column chromatography (SNAP100HP manufactured by Biotage)(hexane/ethyl acetate; 5/1→1/1) to give methyl2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxohexanoate (1.2 g, 91%) asyellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.87 (3H, t, J=7.4 Hz), 1.50-1.55 (2H, m), 2.36-2.68 (2H, m), 3.21-3.27(2H, m), 3.73 (3H, s), 3.84 (1H, t, J=7.6 Hz), 7.50 (1H, td, J=7.6, 1.4Hz), 7.64-7.73 (3H, m), 7.77-7.85 (2H, m), 8.61 (1H, br s).

Process 2: A toluene (45 mL)-acetic acid (5 mL) mixture containingmethyl 2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxohexanoate (1.2 g,3.6 mmol) and ammonium acetate (8.3 g, 108 mmol) was refluxed underheating for 1 hour. After cooling to room temperature, saturated aqueoussolution of sodium hydrogen carbonate was added and extraction wascarried out with toluene. After washing with brine, it was dried overanhydrous sodium sulfate and concentrated in vacuo to give methyl(Z)-3-amino-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-hexenoate (1.15g) as brown oil crude product. It was used for the next process withoutpurification.

Process 3: Isobutyryl chloride (219 mg, 2.06 mmol) and triethylamine(208 mg, 2.06 mmol) were added to 1,2-dichloroethane (10 mL) solution ofmethyl (Z)-3-amino-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-hexenoate(575 mg) and stirred for 16 hours at 50° C. The reaction mixture wasadded water and extracted with chloroform. The organic layer wascombined, washed with brine, dried over anhydrous sodium sulfate, andconcentrated in vacuo. The obtained residues were subjected to silicagel column chromatography (SNAP50HP manufactured by Biotage)(hexane/ethyl acetate; 5/1→1/1) to give methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-hexenoate(158 mg, 23%; two step yield) as black oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.99 (3H, t, J=7.4 Hz), 1.19-1.29 (8H, m), 2.49-2.62 (1H, m), 2.88-2.97(2H, m), 3.71 (3H, s), 3.76 (2H, s), 7.51 (1H, dd, J=7.6, 1.3 Hz), 7.59(1H, dd, J=8.1, 2.1 Hz), 7.64-7.73 (2H, m), 7.77-7.86 (2H, m), 8.60 (1H,s), 11.90 (1H, s).

Process 4: Under argon atmosphere, trimethylaluminum (2 mol/L hexanesolution, 0.39 mL, 0.78 mmol) was added to 1,2-dichloroethane (5 mL)solution of 2-amino-5-ethoxypyrimidine (108 mg, 0.78 mmol) at roomtemperature and stirred for 70 minutes at room temperature.1,2-dichloroethane solution (2 mL) of methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-hexenoate(158 mg, 0.39 mmol) was added dropwise thereto at room temperature andrefluxed under heating for 3 hours. The reaction mixture was added anaqueous solution of ammonium chloride and chloroform, and filteredthrough a pad of celite. The organic layer in the filtrate was separatedand the aqueous layer was extracted with chloroform. The organic layerwas combined, washed with water and brine, dried over anhydrous sodiumsulfate, and concentrated in vacuo. The obtained residues were subjectedto silica gel column chromatography (Flash12M manufactured by Biotage)(chloroform/methanol=40:1) to give2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(111 mg, 58%) as yellow oil.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.97 (3H, t, J=7.4 Hz), 1.17 (6H, d, J=6.6 Hz), 1.49 (3H, t, J=6.9 Hz),1.66-1.77 (2H, m), 2.19-2.32 (1H, m), 2.60-2.70 (2H, m), 3.93 (2H, s),4.10 (2H, q, J=7.1 Hz), 7.45 (1H, td, J=7.7, 1.1 Hz), 7.60-7.67 (2H, m),7.73-7.80 (3H, m), 8.49 (2H, s), 8.67 (1H, d, J=1.3 Hz).

Process 5: Sodium hydrogen carbonate (1.19 g, 14.1 mmol) was added todimethyl sulfoxide (15 mL) mixture of hydroxylamine hydrochloride (838mg, 12.1 mmol) and stirred for 1 hour at 40° C. The reaction mixture wasadded dimethyl sulfoxide (15 mL) solution of2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(353 mg, 0.71 mmol) and stirred for 18 hours at 90° C. The reactionmixture was added water (80 mL) and ethyl acetate (20 mL) and stirredfor 30 minutes. The precipitated solid was collected by filtration andwashed with water and ethyl acetate. It was then dried in vacuo to give2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide(214 mg, 57%) as a white solid.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.98 (3H, t, J=7.3 Hz), 1.19 (6H, d, J=6.6 Hz), 1.51 (3H, t, J=7.0 Hz),1.68-1.78 (2H, m), 2.25-2.32 (1H, m), 2.63-2.70 (2H, m), 3.92 (2H, s),4.22 (2H, q, J=6.9 Hz), 4.72 (2H, br s), 7.40 (1H, td, J=7.5, 1.3 Hz),7.43 (1H, d, J=8.5 Hz), 7.49 (1H, td, J=7.6, 1.5 Hz), 7.55 (1H, dd,J=7.6, 1.2 Hz), 7.58 (1H, dd, J=7.8, 1.2 Hz), 7.66 (1H, dd, J=8.2, 2.3Hz), 8.51 (2H, s), 8.60 (1H, d, J=1.7 Hz).

Process 6: 1,1′-Carbonyldiimidazole (130 mg, 0.80 mmol) and1,8-diazabicyclo[5.4.0]undeca-7-ene (122 mg, 0.80 mmol) were added todichloromethane (4 mL) and tetrahydrofuran (4 mL) mixture solution of2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide(212 mg, 0.40 mmol) and stirred for 3 hours at room temperature. Oncethe reaction is completed, 1 M hydrochloric acid solution was added tothe reaction mixture, which was then extracted with chloroform. Theorganic layer was washed with water, dried over anhydrous sodiumsulfate, and concentrated in vacuo. The obtained residues were subjectedto silica gel column chromatography (chloroform/methanol=20:1) to give3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(201 mg, 91%) as white amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

1.01 (3H, t, J=7.3 Hz), 1.19 (6H, d, J=6.6 Hz), 1.51 (3H, t, J=7.0 Hz),1.71-1.82 (2H, m), 2.26-2.32 (1H, m), 2.66-2.73 (2H, m), 3.95 (2H, s),4.22 (2H, q, J=7.0 Hz), 7.39 (1H, d, J=8.1 Hz), 7.45 (1H, d, J=8.1 Hz),7.51 (1H, t, J=7.6 Hz), 7.60 (1H, t, J=7.7 Hz), 7.83 (1H, dd, J=8.1, 1.7Hz), 7.93 (1H, d, J=7.8 Hz), 8.51 (2H, s), 8.56 (1H, s).

Example 41 Preparation of3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using cyclopropylcarbonyl chloride instead of isobutyrylchloride in the Process 3 of the Example 40, the reaction and thetreatment were performed in the same manner as the Process 3 of theExample 40 to give methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-cyclopropanecarboxyamide-2-hexenoate(yield: 58%).

¹H-NMR(CDCl₃, 400 MHz) δ:

0.83-1.10 (8H, m), 1.58-1.62 (2H, m), 2.87-2.96 (2H, m), 3.71 (3H, s),3.76 (2H, s), 7.49 (1H, td, J=7.6, 1.3 Hz), 7.58 (1H, dd, J=8.1, 2.1Hz), 7.65-7.72 (2H, m), 7.77-7.86 (2H, m), 8.61 (1H, s), 12.15 (1H, s).

Process 2: By using methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-(cyclopropanecarboxyamide)-2-hexenoateinstead of methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-hexenoatein the Process 4 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 40 to give2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 58%).

¹H-NMR (CDCl₃, 400 MHz) δ:

0.80-0.87 (2H, m), 0.96 (3H, t, J=7.5 Hz), 1.08-1.14 (1H, m), 1.21-1.25(2H, m), 1.51 (3H, t, J=7.0 Hz), 1.61-1.72 (2H, m), 2.57-2.61 (2H, m),3.94 (2H, s), 4.22 (2H, q, J=6.9 Hz), 7.47 (1H, td, J=7.6, 1. Hz),7.63-7.69 (2H, m), 7.74-7.82 (3H, m), 8.54 (2H, s), 8.68 (1H, d, J=1.8Hz).

Process 3: By using2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-1-yl)-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 5 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 5 of the Example 40 to give2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide(yield: 67%).

¹H-NMR (CDCl₃, 400 MHz) δ:

0.79-0.88 (2H, m), 0.94 (3H, t, J=7.4 Hz), 1.06-1.15 (1H, m), 1.19-0.26(2H, m), 1.51 (3H, t, J=7.1 Hz), 1.59-1.71 (2H, m), 2.53-2.64 (2H, m),3.91 (2H, s), 4.22 (2H, q, J=7.0 Hz), 4.73 (2H, s), 7.40 (1H, td, J=7.3,1.6 Hz), 7.43 (1H, d, J=7.6 Hz), 7.49 (1H, td, J=7.6, 1.5 Hz), 7.55 (1H,dd, J=7.6, 1.0 Hz), 7.58 (1H, dd, J=7.7, 0.9 Hz), 7.64 (1H, dd, J=8.2,2.3 Hz), 8.54 (2H, s), 8.59 (1H, d, J=2.2 Hz).

Process 4: By using2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 6 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 6 of the Example 40 to give3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 94%) as white amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.81-0.89 (1H, m), 0.97 (3H, t, J=7.4 Hz), 1.06-1.15 (1H, m), 1.21-1.27(2H, m), 1.51 (3H, t, J=7.0 Hz), 1.66-1.70 (2H, m), 2.61 (2H, t, J=7.4Hz), 3.94 (2H, s), 4.22 (2H, q, J=6.8 Hz), 7.39 (1H, d, J=0.3 Hz), 7.45(1H, d, J=7.6 Hz), 7.52 (1H, t, J=7.6 Hz), 7.60 (1H, t, J=7.2 Hz), 7.81(1H, dd, J=7.9, 1.8 Hz), 7.94 (1H, d, J=7.8 Hz), 8.54 (2H, s), 8.55 (1H,s).

Example 42 Preparation of3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using methyl 3-oxooctanoate instead of methyl3-oxohexanoate in the Process 1 of the Example 40, the reaction and thetreatment were performed in the same manner as the Process 1 of theExample 40 to give methyl2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxooctanoate (yield: 38%).

¹H-NMR (CDCl₃, 400 MHz) δ:

0.86 (3H, t, J=6.9 Hz), 1.19-1.32 (4H, m), 1.49-1.55 (2H, m), 2.35-2.67(2H, m), 3.20-3.26 (2H, m), 3.73 (3H, s), 3.84 (1H, t, J=7.4 Hz), 7.50(1H, td, J=7.6, 1.3 Hz), 7.64-7.73 (3H, m), 7.77-7.85 (2H, m), 8.61 (1H,br s).

Process 2: By using methyl2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxooctanoate instead ofmethyl 2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxohexanoate in theProcess 2 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 40 to givemethyl (Z)-3-amino-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-octenoate(yield: 82%) as brown oil crude product. It was used for the nextprocess without purification.

Process 3: By using methyl(Z)-3-amino-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-octenoateinstead of methyl(Z)-3-amino-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-hexenoate in theProcess 3 of the Example 40, the reaction was performed in the samemanner as the Process 3 of the Example 40. According to a post-treatmentcarried out in the same manner as the Process 3 of the Example 40,methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-octenoatewas obtained as a crude product. It was used for the next processwithout purification.

Process 4: By using methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-octenoateinstead of methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-hexenoatein the Process 4 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 40 to give2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 86%).

¹H-NMR (CDCl₃, 400 MHz) δ:

0.90 (3H, t, J=6.8 Hz), 1.20 (6H, d, J=6. Hz), 1.32-1.39 (4H, m), 1.51(3H, t, J=7.0 Hz), 1.65-1.75 (2H, m), 2.24-2.33 (1H, m), 2.65-2.71 (2H,m), 3.95 (2H, s), 4.22 (2H, q, J=7.0 Hz), 7.47 (1H, td, J=7.6, 1.1 Hz),7.63-7.69 (2H, m), 7.76-7.82 (3H, m), 8.51 (2H, s), 8.70 (1H, d, J=1.5Hz).

Process 5: By using2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 5 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 5 of the Example 40 to give2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide(yield: 59%).

¹H-NMR (CDCl₃, 400 MHz) δ:

0.90 (3H, t, J=7.0 Hz), 1.21 (6H, t, J=12.2 Hz), 1.30-1.39 (4H, m), 1.51(3H, t, J=7.0 Hz), 1.65-1.74 (2H, m), 2.25-2.32 (1H, m), 2.68 (2H, t,J=7.6 Hz), 3.92 (2H, s), 4.22 (2H, q, J=7.0 Hz), 4.73 (2H, br s), 7.40(1H, td, J=7.6, 1.4 Hz), 7.43 (1H, d, J=8.5 Hz), 7.49 (1H, td, J=7.5,1.3 Hz), 7.55 (1H, dd, J=7.6, 1.2 Hz), 7.58 (1H, dd, J=7.6, 12 Hz), 7.66(1H, dad, J=8.2, 2.3 Hz), 8.51 (2H, s), 8.59 (1H, d, J=2.0 Hz).

Process 6: By using2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 6 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 6 of the Example 40 to give3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-pentyl-1,6-dihydropyrimidin-1-yl]methyl}pyridin-2-yl}phenyl}1,2,4-oxadiazol-5(4H)-one(yield: 99%).

¹H-NMR (CDCl₃, 400 MHz) δ:

0.90 (3H, t, J=7.0 Hz), 1.20 (6H, d, J=6.6 Hz), 1.31-1.42 (4H, m), 1.51(3H, t, J=7.1 Hz), 1.67-1.77 (2H, m), 2.26-2.32 (1H, m), 2.71 (2H, t,J=7.6 Hz), 3.95 (2H, s), 4.22 (2H, q, J=7.0 Hz), 7.41 (1H, d, J=8.1 Hz),7.45 (1H, dd, J=7.8, 1.2 Hz), 7.53 (1H, td, J=7.7, 1.2 Hz), 7.61 (1, td,J=7.6, 1.5 Hz), 7.84 (1H, d, J=8.3 Hz), 7.97 (1H, d, J=7.6 Hz), 8.51(2H, s), 8.59 (1H, s).

Example 43 Preparation of3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using cyclopropanecarbonyl chloride instead of isobutyrylchloride in the Process 3 of the Example 40 and also using methyl(Z)-3-amino-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-octenoateinstead of methyl(Z)-3-amino-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-hexenoate, thereaction was performed in the same manner as the Process 3 of theExample 40. According to a post-treatment carried out in the same manneras the Process 3 of the Example 40, methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-cyclopropanecarboxamide-2-octenoatewas obtained as a crude product. It was used for the next processwithout purification.

Process 2: By using methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-cyclopropanecarboxamide-2-octenoateinstead of methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-hexenoatein the Process 4 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 40 to give2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 64%).

¹H-NMR (CDCl₃, 400 MHz) δ:

0.81-0.91 (5H, m), 1.07-1.14 (1H, m), 1.21-1.26 (2H, m), 1.29-1.36 (4H,m), 1.49-1.53 (3H, m), 1.60-1.65 (2H, m), 2.57-2.6 (2H, m), 3.94 (2H,s), 4.2 (2H, q, J=7.1 Hz), 7.44-7.50 (1H, m), 7.63-7.69 (2H, m),7.73-7.83 (3H, m), 8.54 (2H, s), 8.69 (1H, s).

Process 3: By using2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 5 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 5 of the Example 40 to give2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxyhenzimidamide(yield: 70%).

¹H-NMR, (CDCl₃, 400 MHz) δ:

0.81-0.86 (2H, m), 0.89 (3H, t, J=6.8 Hz), 1.06-1.15 (1H, m), 1.19-1.25(2H, m), 1.28-1.35 (4H, m), 1.51 (3H, t, J=7.1 Hz), 1.58-1.65 (2H, m),2.60 (2H, t, J=7.9 Hz), 3.90 (2H, s), 4.22 (2H, q, J=7.0 Hz), 4.73 (2H,br s), 7.40 (1H, td, J=7.5, 1.5 Hz), 7.43 (1H, d, J=7.8 Hz), 7.49 (1H,td, J=7.6, 1.5 Hz), 7.55 (1H, dd, J=7.6, 1.5 Hz), 7.58 (1H, dd, J=7.9,1.1 Hz), 7.64 (1H, dd, J=8.1, 2.4 Hz), 8.54 (2H, s), 8.58 (1H, d, J=1.7Hz).

Process 4: By using2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 6 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 6 of the Example 40 to give3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-6-oxo-4-pentyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 91%) as white amorphous.

¹H-NMR, (CDCl₃, 400 MHz) δ:

0.82-0.93 (5H, m), 1.07-1.15 (1H, m), 1.1-1.27 (2H, m), 1.29-1.38 (4H,m), 1.51 (3H, t, J=7.0 Hz), 1.59-1.70 (2H, m), 2.62 (2H, t, J=7.7 Hz),3.93 (2H, s), 4.22 (2H, q, J=7.0 Hz), 7.40 (1H, d, J=7.8 Hz), 7.45 (1,d, J=7.6 Hz), 7.53 (1H, td, J=7.6, 1.2 Hz), 7.61 (1H, td, J=7.7, 1.4Hz), 7.81 (1H, ad, J=7.9, 2.1 Hz), 7.96 (1H, d, J=7.8 Hz), 8.54 (2H, s),8.57 (1H, s), 7.60 (1H, t, J=7.2 Hz), 7.81 (1H, dd, J=7.9, 1.5 Hz), 7.94(1H, d, J=7.8 Hz), 8.54 (2H, s), 8.55 (1H, s).

Example 44 Preparation of3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-4-ethyl-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using methyl 3-oxopentanoate instead of methyl3-oxohexanoate in the Process 1 of the Example 40, the reaction and thetreatment were performed in the same manner as the Process 1 of theExample 40 to give2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxopentanoate (yield: 43%).

¹H-NMR (CDCl₃, 400 MHz) δ:

1.05 (3H, t, J=7 Hz), 2.44 (1H, dq, J=22, 7 Hz), 2.66 (1H, dq, J=22, 7Hz), 3.24 (2H, dd, J=7, 7 Hz), 3.73 (3H, s), 3.84 (1H, t, J=7 Hz), 7.50(1H, dd, J=8, 1 Hz), 7.67-7.70 (3H, m), 7.78 (1H, d, J=8 Hz), 7.83 (1H,d, J=8 Hz), 8.60 (1H, d, J=2 Hz).

Process 2: By using methyl2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxopentanoate instead ofmethyl 2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-oxohexanoate in theProcess 2 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 2 of the Example 40 to givemethyl(Z)-3-amino-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-pentenoate as acrude product. It was used for the next process without purification.

Process 3: By using methyl(Z)-3-amino-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-pentenoateinstead of methyl(Z)-3-amino-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-hexenoate in theProcess 3 of the Example 40, the reaction was performed in the samemanner as the Process 3 of the Example 40. According to a post-treatmentcarried out in the same manner as the Process 3 of the Example 40,methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-pentenoate(two step yield: 3.3%) was obtained as a crude product.

¹H-NMR (CDCl₃, 400 MHz) δ:

1.17 (3H, t, J=7 Hz), 1.25 (6H, c, J=7 Hz), 2.57 (1H, sept, J=7 Hz), 3.0(2H, q, J=7 Hz), 3.71 (3H, s), 3.77 (2H, s), 7.49 (1H, dd, J=8, 1 Hz),7.60 (1H, dd, J=8, 2 Hz), 7.70 (2H, m), 7.79 (1H, d, J=8 Hz), 7.83 (1H,d, J=8 Hz), 8.61 (1H, d, J=2 Hz), 11.9 (1H, s).

Process 4: By using methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-pentenoateinstead of methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-hexenoatein the Process 4 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 40 to give2-{5-{[1-(5-ethoxypyrimidin-2-yl)-4-ethyl-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 58%).

¹H-NMR (CDCl₃, 400 MHz) δ:

1.20 (6H, d, J=7 Hz), 1.25 (3H, t, J=8 Hz), 1.52 (3H, t, J=7 Hz), 2.29(1H, sept, J=7 Hz), 2.72 (2H, q, J=8 Hz), 4.0 (2H, s), 4.21 (2H, q, J=7Hz), 7.47 (1H, dd, J=8, 1 Hz), 7.64-7.68 (2H, m), 7.76-7.78 (3H, m),8.51 (2H, s), 8.70 (1H, d, J=2 Hz).

Process 5: By using2-{5-{[1-(5-ethoxypyrimidin-2-yl)-4-ethyl-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 5 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 5 of the Example 40 to give2-{5-{[1-(5-ethoxypyrimidin-2-yl)-4-ethyl-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamide(yield: 61%).

¹H-NMR (CDCl₃, 400 MHz) δ:

1.19 (6H, d, J=7 Hz), 1.22 (3H, t, J=8 Hz), 1.50 (3H, t, J=7 Hz), 2.29(1H, sept, J=7 Hz), 2.69 (2H, q, J=8 Hz), 3.91 (2H, s), 4.20 (2H, q, J=7Hz), 4.78 (2H, br), 7.37-7.40 (2H, m), 7.44-7.51 (2H, m), 7.56 (1H, dd,J=8, 1 Hz), 7.63 (1H, dd, J=, 2 Hz), 8.50 (2H, s), 8.57 (1H, d, J=2 Hz).

Process 6: By using2-{5-{[1-(5-ethoxypyrimidin-2-yl)-4-ethyl-2-isopopyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 6 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 6 of the Example 40 to give3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-4-ethyl-2-isopropyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 56%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

1.19 (6H, d, J=7 Hz), 1.24 (3H, t, J=8 Hz), 1.51 (3H, t, J=7 Hz), 2.28(1H, sept, J=7 Hz), 2.69 (2H, q, J=8 Hz), 3.93 (2H, s), 4.22 (2H, q, J=7Hz), 7.30 (1H, d, J=8 Hz), 7.37-7.41 (2H, m), 7.49 (1H, d, J=8, 1 Hz),7.67 (1H, d, J=8 Hz), 7.77 (1H, dd, J=8, 2 Hz), 8.39 (1H, d, J=2 Hz),8.51 (2H, s).

Example 45 Preparation of3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-4-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one

Process 1: By using cyclopropanecarbonyl chloride instead of isobutyrylchloride in the Process 3 of the Example 40 and also using methyl(Z)-3-amino-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-pentenoateinstead of methyl(Z)-3-amino-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-2-hexenoate, thereaction was performed in the same manner as the Process 3 of theExample 40. According to a post-treatment carried out in the same manneras the Process 3 of the Example 40, methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-cyclopropanecarboxamide-2-pentenoate(two step yield: 3.7%) was obtained as a crude product.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.85-0.90 (2H, m), 1.05-1.08 (3H, m), 1.16 (3H, t, J=8 Hz), 2.98 (2H, q,J=8 Hz), 3.72 (3H, s), 3.77 (2H, s), 7.49 (1H, dd, J=8, 1 Hz), 7.59 (1H,dd, J=8, 2 Hz), 7.66-7.72 (2H, m), 7.79 (1H, d, J=8 Hz), 7.83 (1H, d,J=8 Hz), 8.62 (1H, d, J=2 Hz), 12.1 (1H, s).

Process 2: By using methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-cyclopropanecarboxamide-2-pentenoateinstead of methyl(Z)-2-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-3-isobutylamide-2-hexenoatein the Process 4 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 4 of the Example 40 to give2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-4-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrile(yield: 13%)

¹H-NMR (CDCl₃, 400 MHz) δ:

0.82-0.88 (2H, m), 1.08-1.15 (1H, m), 1.18 (3H, t, J=8 Hz), 1.23-1.28(2H, m), 1.50 (3H, t, J=7 Hz), 2.63 (2H, q, J=8 Hz), 3.95 (2H, s), 4.21(2H, q, J=7 Hz), 7.44-7.48 (1H, m), 7.64-7.66 (2H, m), 7.76-7.78 (3H,m), 8.53 (2H, s), 8.7 (1H, d, J=2 Hz).

Process 3: By using2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-4-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrileinstead of2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}benzonitrilein the Process 5 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 5 of the Example 40 to give2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-4-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimiidamide(yield: 52%).

¹H-NMR (CDCl₃, 400 MHz) δ:

0.82-0.88 (2H, m), 1.04-1.12 (1H, m), 1.15 (3H, t, J=8 Hz), 1.22-1.28(2H, m), 1.50 (3H, t, J=7 Hz), 2.62 (2H, g, J=8 Hz), 3.90 (2H, s), 4.21(2H, q, J=7 Hz), 4.76 (2H, br), 7.38-7.40 (2H, m), 7.47-7.51 (2H, m),7.57 (1H, d, J=8 Hz), 7.61 (1H, d, J=8 Hz), 8.53 (2H, s), 8.57 (1H, s).

Process 4: By using2-{5-{[2-cyclopropyl-1-(ethoxypyrimidin-2-yl)-4-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamideinstead of2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}-N′-hydroxybenzimidamidein the Process 6 of the Example 40, the reaction and the treatment wereperformed in the same manner as the Process 6 of the Example 40 to give3-{2-{5-{[2-cyclopropyl-1-(5-ethoxypyrimidin-2-yl)-4-ethyl-6-oxo-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one(yield: 45%) as pale yellow amorphous.

¹H-NMR (CDCl₃, 400 MHz) δ:

0.82-0.90 (2H, m), 1.08-1.11 (1H, m), 1.18 (3H, t, J=8 Hz), 1.23-1.26(2H, m), 1.51 (3H, t, J=7 Hz), 2.63 (2H, q, J=8 Hz), 3.91 (2H, s), 4.21(2H, q, J=7 Hz), 7.31 (1H, d, J=8 Hz), 7.37-7.44 (2H, m), 7.51 (1H, dd,J=8, 2 Hz), 7.73 (1H, d, J=8 Hz), 7.76 (1H, dd, J=8, 2 Hz), 8.40 (1H, d,J=2 Hz), 8.54 (2H, s)

Test Example 1 Angiotensin II Antagonistic Activity in Isolated RabbitBlood Vessels

By using a specimen of isolated rabbit blood vessels, antagonisticactivity of the compounds of the invention against angiotensin II type 1receptor was calculated from a dose-response curve of angiotensinII-induced blood vessel contraction. Specifically, the specimen ofthoracic aorta ring of a rabbit (New Zealand White: male, 2.4 to 3.0 kg)was suspended in a rmagnus bath filled with Krebs-Henseleite buffer(composition: 118 mM NaCl, 4.7 mM KCl, 2.55 mM CaCl₂, 1.18 mM MgSO₄,1.18 mM KH₂PO₄, 24.88 mM NaHCO₃, and 11.1 mM D-glucose), and angiotensinII (10 n M)-induced contraction was obtained in the presence of eachtest compound (1 n mol/L to 10 μmol/L). During the measurement, theinside temperature of the magnus bath was maintained at 37° C. and thebath was continuously ventilated with a sufficient amount of mixed gas(95% O₂ and 5% CO₂). The angiotensin II-induced contraction wasconverted into a relative value (%) that is based on the angiotensin II(0.1 μM)-induced contraction in the absence of the test compound.

As a result, it was confirmed that the compounds described in theExamples have an angiotensin II antagonistic activity at theconcentration of 0.1 μM. The inhibitory rate of angiotensin II (10 nM)at the test compound concentration of 0.1 μM is shown in the Table 1. Asshown in the Table 1, it was confirmed that the compounds of theinvention have a potent angiotensin II antagonistic activity, which isthe same as telmisartan. Meanwhile, under the same condition, rate ofinhibiting the angiotensin II activity by telmisartan was 85.3%.

TABLE 1 Rate (%) of inhibiting angiotensin II activity at Example No.concentration of 0.1 μM 1 100 2 90.8 12 100 13 100 14 59.3 15 78.3 1672.9 17 52.1 21 70.3 22 59.5 23 75.2 28 86.5 29 96.3 40 68.3 41 89.9

Test Example 2 PPARγ Activation Effect

The agonistic activity of the compounds of the invention on PPARγ wasmeasured based on the transfection assay using COS7 cells (DS PharmaBiomedical Co., Ltd., Osaka, Japan), which are the cell line derivedfrom the kidney of the African green monkey. COS7 cells were culturedunder 5% CO₂ concentration, and DMEM medium containing 10% fetal bovineserum, glutamic acid, and antibiotics was used as a medium.

As an expression vector, a chimera in which DNA binding domain of Gal4,which is a yeast transcription factor, and ligand binding domain ofhuman PPARγ2 are fused, i.e., a fused product between the amino acids 1to 147 of Gal4 transcription factor and the amino acids 182 to 505 ofhuman PPARγ2, was used. Furthermore, as a reporter vector, a fireflyluciferase containing five copies of Gal4 recognition sequence in thepromoter region was used. Plasmid transfection to the cells wasperformed according to a method which uses jetPEI (trade name,manufactured by Funakoshi Co., Ltd., Tokyo, Japan). Furthermore,β-galactosidase expression vector was employed as an internal standard.

After the transfection into the cells, the medium was replaced with aDMEM medium (containing 1% serum) added with the test compound, and thecells were further cultured for 16 hours. After that, the luciferaseactivity and β-galactosidase activity in the cell lysis solution weremeasured.

Meanwhile, for the present test, dimethylsulfoxide (DMSO) was used fordissolution and dilution of the test compounds, and during the celltreatment, the DMSO concentration in DMEM medium (containing 1% serum)was adjusted to 0.1%. As a positive compound, rosiglitazone (trade name,manufactured by ALEXIS Corporation, Switzerland) was used. Thepercentage (%) of the luciferase activity of the each test compound (1to 30 μmol/L) was calculated when the luciferase activity ofrosiglitazone (3 to 10 μmol/L) is 100% and the luciferase activity inthe absence of the test compound is 0%. The 50% effective concentrationof the test compound (EC₅₀, 50% effect concentration) was calculated byusing SAS Preclinical Package Ver 5.0 (trade name, manufactured by SASinstitute Japan Co., Tokyo, Japan), which is a statistical analysisprogram.

As a result, it was confirmed that the compounds described in theExamples have a PPARγ activation effect at the concentration of 30 μM.The EC₅₀ results are given in the Table 2. As shown in the Table 2, itwas confirmed that the compounds of the invention have a potent PPARγactivation effect. In particular, several compounds in the Table 2exhibited EC₅₀ value of less than 1 μM, indicating stronger PPARγactivation effect than telmisartan. Maximum activity strength of severalcompounds relative to the maximum activity of rosiglitazone is given inthe Table 3. As shown in Table 3, it was confirmed that the compounds ofthe invention have an activity that is 20 to 69% of the maximum activityof rosiglitazone and they have a sufficient agonist activity on PPARγ.In particular, the maximum activity of the compounds of the Examples 40,41, 42, and 43 was 42 to 69%, which is the same or greater than that oftelmisartan. Under the same condition, the PPARγ activation effect oftelmisartan, i.e., EC₅₀, was 1 to 5 μM, and the maximum activitystrength of telmisartan relative to the maximum activity ofrosiglitazone (i.e., % MAX vs. rosiglitazone) was 30 to 50%.

TABLE 2 Example No. EC₅₀ (μM) 6 1.36 15 3.61 17 3.12 18 3.39 19 1.50 200.85 21 0.45 22 1.55 23 0.76 24 1.46 25 0.82 26 0.38 27 0.67 32 2.74 400.40 41 0.56 42 0.65 43 0.59

TABLE 3 % MAX vs Example No. Rosiglitazone 40 69 41 65 42 53 43 42

From the results obtained above, it was confirmed that the compounds ofthe present invention have both a potent angiotensin II receptorantagonistic activity and a PPARγ activation effect. Thus, it was foundthat the compounds of the present invention and pharmaceuticallyacceptable salts thereof are useful as an effective component of aprophylactic and/or therapeutic agent for disorders involved withangiotensin II and PPARγ, for example, hypertension, heart diseases,angina pectoris, cerebral vascular disorders, cerebral circulatorydisorders, ischemic peripheral circulatory disorders, renal diseases,arteriosclerosis, inflammatory diseases, type 2 diabetes, diabeticcomplications, insulin resistance syndrome, syndrome X, metabolicsyndrome, and hyperinsulinemia.

INDUSTRIAL APPLICABILITY

The phenylpyridine derivatives represented by the formula (I) of theinvention or salts thereof, or solvates thereof are a novel compoundwhich have both an angiotensin II receptor antagonistic activity and aPPARγ activation effect, and the present invention provides the novelcompounds and a pharmaceutical composition containing the same. Thecompounds of the invention are used as an effective component of a novelpharmaceutical product, i.e., a prophylactic and/or therapeutic agentfor disorders involved with angiotensin II and PPARγ, for example,hypertension, heart diseases, angina pectoris, cerebral vasculardisorders, cerebral circulatory disorders, ischemic peripheralcirculatory disorders, renal diseases, arteriosclerosis, inflammatorydiseases, type 2 diabetes, diabetic complications, insulin resistancesyndrome, syndrome X, metabolic syndrome, and hyperinsulinemia, andtherefore have an industrial applicability.

The invention claimed is:
 1. A compound which is3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-one,or a salt thereof, or a solvate thereof.
 2. A method of treating acirculatory disease, the method comprising administering an effectiveamount of3-{2-{5-{[1-(5-ethoxypyrimidin-2-yl)-2-isopropyl-6-oxo-4-propyl-1,6-dihydropyrimidin-5-yl]methyl}pyridin-2-yl}phenyl}-1,2,4-oxadiazol-5(4H)-oneor a salt or solvate thereof to a patient who is in need of thetreatment.
 3. The method of treating a circulatory disease according toclaim 2, wherein the circulatory disease is hypertension, heart disease,angina pectoris, cerebral vascular disorder, cerebral circulatorydisorder, ischemic peripheral circulatory disorder, kidney disease, orarteriosclerosis.